Canonical Allele Identifier: PA2826465680
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 420561

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val774Ala
CA16617604
NM_001258281.1:c.2321T>C