Canonical Allele Identifier: PA2826463169
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 919342
ClinVar RCV Id: RCV001177474 RCV001875849 RCV004006387
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala164Asp
CA346731907
NM_001258281.1:c.491C>A