Canonical Allele Identifier: PA297099
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 181503
ClinVar RCV Id: RCV000159056 RCV001002766 RCV002515083 RCV001261020 RCV001813411 RCV003764999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Pro491Ala
CA297097
NM_002834.5:c.1471C>G