Canonical Allele Identifier: PA2826625266
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1768455
ClinVar RCV Id: RCV002387363 RCV003759658
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile199Thr
CA346741074
NM_001281492.2:c.596T>C