Canonical Allele Identifier: PA2826464180
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408520
ClinVar RCV Id: RCV000561959 RCV000463668 RCV001753886 RCV004000788
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.His400Arg
CA028501
NM_001258281.1:c.1199A>G