Canonical Allele Identifier: PA2579908967
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2831395
ClinVar RCV Id: RCV003758272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala14Glu
CA346728534
NM_000251.3:c.41C>A