Canonical Allele Identifier: PA331216
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90516
ClinVar RCV Id: RCV000629705 RCV002408591 RCV003460713
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu357Gln
CA017022
NM_000251.3:c.1069G>C