Canonical Allele Identifier: PA2826625954
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2107070
ClinVar RCV Id: RCV003026792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala364Gly
CA346746045
NM_001281492.2:c.1091C>G