Canonical Allele Identifier: PA645381221
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410524
ClinVar RCV Id: RCV000458338 RCV000562905 RCV004001856 RCV002281095
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp649Gly
CA16610993
NM_000179.3:c.1946A>G