Canonical Allele Identifier: PA2826632812
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1692256
ClinVar RCV Id: RCV002257122
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro775Ala
CA346758037
NM_001281493.2:c.2323C>G