Canonical Allele Identifier: PA2826629669
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1171277
ClinVar RCV Id: RCV001524238 RCV001872024
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro41His
CA346741378
NM_001281493.2:c.122C>A