Canonical Allele Identifier: PA299521
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182661
ClinVar RCV Id: RCV000160717 RCV000409643 RCV000570608 RCV000629702 RCV001354913 RCV001582637 RCV003998511
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser806Cys
CA010210
NM_000179.3:c.2417C>G