Canonical Allele Identifier: PA2826637810
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1734675
ClinVar RCV Id: RCV002363847
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu952Lys
CA346761099
NM_001281494.2:c.2854G>A