Canonical Allele Identifier: PA2826465007
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90852
ClinVar RCV Id: RCV000076354 RCV001854322 RCV002415559 RCV003452878
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly603Asp
CA019774
NM_001258281.1:c.1808G>A