Canonical Allele Identifier: PA2826463419
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1426650
ClinVar RCV Id: RCV001949777 RCV002442883
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln222His
CA346732864
NM_001258281.1:c.666G>C
CA346732865
NM_001258281.1:c.666G>T