Canonical Allele Identifier: PA2826628943
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185667
ClinVar RCV Id: RCV000165125 RCV000459296 RCV001527033 RCV003995394
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala1131Val
CA014254
NM_001281492.2:c.3392C>T