Canonical Allele Identifier: PA2825089499
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2587343
ClinVar RCV Id: RCV003360821
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu778Pro
CA346753385
NM_000179.3:c.2333T>C