Canonical Allele Identifier: PA1139674945
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 957715
ClinVar RCV Id: RCV001230742
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys775Gln
CA068824
NM_000179.3:c.2323A>C