Canonical Allele Identifier: PA658680954
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483798
ClinVar RCV Id: RCV000573544
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp790His
CA346753665
NM_000179.3:c.2368G>C