Canonical Allele Identifier: PA645476331
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 234060
ClinVar RCV Id: RCV000217786 RCV000698616
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu902Asp
CA10578014
NM_000251.3:c.2706A>C
CA346731691
NM_000251.3:c.2706A>T