Canonical Allele Identifier: PA658680594
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483857
ClinVar RCV Id: RCV000575116 RCV002298682
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys476Arg
CA346745443
NM_000179.3:c.1427A>G