Canonical Allele Identifier: PA645382827
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232656
ClinVar RCV Id: RCV000220173 RCV003765429
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp936Asn
CA10578119
NM_000179.3:c.2806G>A