Canonical Allele Identifier: PA2826463231
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1948616
ClinVar RCV Id: RCV002667872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu178Phe
CA346732200
NM_001258281.1:c.534G>C
CA346732201
NM_001258281.1:c.534G>T