Canonical Allele Identifier: PA2827312832
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40502
ClinVar RCV Id: RCV000033478 RCV000037639 RCV000254683 RCV000762884 RCV001813246 RCV003150934
ClinVar Variation Id: 40503
ClinVar RCV Id: RCV000037638 RCV000033479 RCV000856760 RCV000472904 RCV002453282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Glu76Asp
CA261577
NM_001330437.2:c.228G>C
CA261580
NM_001330437.2:c.228G>T