Canonical Allele Identifier: PA2579912984
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1759505
ClinVar RCV Id: RCV002394005

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln252Leu
CA346732348
NM_000251.3:c.755A>T