Canonical Allele Identifier: PA2826632123
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 956342
ClinVar RCV Id: RCV001229127 RCV002436888
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ala613Val
CA346755404
NM_001281493.2:c.1838C>T