Canonical Allele Identifier: PA2826625774
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1519149
ClinVar RCV Id: RCV002043647
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu319Met
CA346744609
NM_001281492.2:c.955C>A