Canonical Allele Identifier: PA2828530853
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 561713
ClinVar RCV Id: RCV000681078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361554.1:p.Glu522Asp
CA386780067
NM_001374625.1:c.1566A>C
CA386780069
NM_001374625.1:c.1566A>T