Canonical Allele Identifier: PA330633
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89575
ClinVar RCV Id: RCV001019736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala326Val
CA016705
NM_000179.3:c.977C>T