Canonical Allele Identifier: PA2826628541
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 938809
ClinVar RCV Id: RCV001208100
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu1047Arg
CA346760230
NM_001281492.2:c.3140T>G