Canonical Allele Identifier: PA2825089050
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1783525
ClinVar RCV Id: RCV002423397
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro656Ala
CA346750592
NM_000179.3:c.1966C>G