Canonical Allele Identifier: PA2826464726
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90791
ClinVar RCV Id: RCV000076292 RCV001854317 RCV002408595 RCV003460714
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asp537Gly
CA019354
NM_001258281.1:c.1610A>G