Canonical Allele Identifier: PA2826463380
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1049766
ClinVar RCV Id: RCV001356290 RCV002547631
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu213Pro
CA46683995
NM_001258281.1:c.638T>C