Canonical Allele Identifier: PA2828530829
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40561
ClinVar RCV Id: RCV000033548 RCV000532971 RCV000677651 RCV001330778 RCV002490448 RCV003450655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361554.1:p.Gly502Glu
CA282132
NM_001374625.1:c.1505G>A