Canonical Allele Identifier: PA2826465531
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_001245210.1:p.Asn732Ser
CA020537
NM_001258281.1:c.2195A>G