Canonical Allele Identifier: PA2826636215
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 924494
ClinVar RCV Id: RCV001185858

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Pro514Arg
CA346754062
NM_001281494.2:c.1541C>G