Canonical Allele Identifier: PA2826631506
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237155
ClinVar RCV Id: RCV000234432 RCV000418671 RCV000758668 RCV001015160
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg470Gln
CA068814
NM_001281493.2:c.1409G>A