Canonical Allele Identifier: PA2826463840
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 449782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro319Ala
CA46702663
NM_001258281.1:c.955C>G