Canonical Allele Identifier: PA2826624848
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142525
ClinVar RCV Id: RCV000131704 RCV000212633 RCV000557767 RCV000663288 RCV003467182 RCV003998115
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro103Arg
CA016269
NM_001281492.2:c.308C>G