Canonical Allele Identifier: PA2826636630
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455216
ClinVar RCV Id: RCV000560703 RCV000566003 RCV000708881 RCV001558112 RCV003459170
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg609Gln
CA069556
NM_001281494.2:c.1826G>A