Canonical Allele Identifier: PA334062
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 188109
ClinVar RCV Id: RCV000167962 RCV000773069 RCV000986688 RCV001762391
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn798Ser
CA020537
NM_000251.3:c.2393A>G