Canonical Allele Identifier: PA2826625796
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 418322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asn325Lys
CA16617650
NM_001281492.2:c.975C>G
CA346744819
NM_001281492.2:c.975C>A