Canonical Allele Identifier: PA2826626203
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234200
ClinVar RCV Id: RCV000215555 RCV000463760 RCV001753682 RCV003998606
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.His422Gln
CA067967
NM_001281492.2:c.1266T>A
CA346747303
NM_001281492.2:c.1266T>G