Canonical Allele Identifier: PA2825089454
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2676794
ClinVar RCV Id: RCV003470248
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro768His
CA068802
NM_000179.3:c.2303C>A