Canonical Allele Identifier: PA2827313109
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13328
ClinVar RCV Id: RCV000030620 RCV000033504 RCV000055890 RCV000077859 RCV000577894 RCV000617951 RCV000492270 RCV000768062 RCV001000775 RCV000824744 RCV001813194 RCV004528108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Tyr279Cys
CA220149
NM_001330437.2:c.836A>G