Canonical Allele Identifier: PA190147
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184819
ClinVar RCV Id: RCV000164144 RCV000629676
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu220Ala
CA016166
NM_000179.3:c.659A>C