Canonical Allele Identifier: PA2826626079
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230508
ClinVar RCV Id: RCV004520659
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser395Ile
CA346746814
NM_001281492.2:c.1184G>T