Canonical Allele Identifier: PA2828530494
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1305307
ClinVar RCV Id: RCV001768514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361554.1:p.Thr167Ser
CA386781838
NM_001374625.1:c.499A>T
CA386781842
NM_001374625.1:c.500C>G