Canonical Allele Identifier: PA2826463208
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 826879
ClinVar RCV Id: RCV001026108
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln173Pro
CA346732090
NM_001258281.1:c.518A>C