Canonical Allele Identifier: PA284664
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 55797
ClinVar RCV Id: RCV000049228 RCV000414941 RCV001813372 RCV002287357 RCV002513672 RCV003224860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Gly60Val
CA284662
NM_002834.5:c.179G>T