Canonical Allele Identifier: PA2827312778
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13333
ClinVar RCV Id: RCV000014261 RCV000077857 RCV000033468 RCV000157000 RCV000515408 RCV000588678 RCV000722014 RCV001249667 RCV001813198 RCV003147286 RCV003137518 RCV004528109
ClinVar Variation Id: 372674
ClinVar RCV Id: RCV000413931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Tyr63Cys
CA220146
NM_001330437.2:c.188A>G
CA16042834
NM_001330437.2:c.188_189delinsGC