Canonical Allele Identifier: PA2827313180
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 372668
ClinVar RCV Id: RCV000412738 RCV000701867 RCV002318367 RCV002481274 RCV004544723
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Met311Val
CA6798676
NM_001330437.2:c.931A>G