Canonical Allele Identifier: PA2827313209
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 181501
ClinVar RCV Id: RCV000159054 RCV001850235
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Cys333Ser
CA297091
NM_001330437.2:c.997T>A
CA386791356
NM_001330437.2:c.998G>C