Canonical Allele Identifier: PA2826465323
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246264
ClinVar RCV Id: RCV000236064 RCV000556812 RCV000564620 RCV003469187 RCV003998917
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asp676Asn
CA10584222
NM_001258281.1:c.2026G>A