Canonical Allele Identifier: PA287352
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser309Cys
CA016656
NM_000179.3:c.926C>G