Canonical Allele Identifier: PA2826464916
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 186196
ClinVar RCV Id: RCV000165743 RCV000529191 RCV003332132
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu581Gln
CA019596
NM_001258281.1:c.1741G>C