Canonical Allele Identifier: PA2825087524
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2453218
ClinVar RCV Id: RCV003182673

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser328Asn
CA346741053
NM_000179.3:c.983G>A