Canonical Allele Identifier: PA2826631648
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2133600
ClinVar RCV Id: RCV003064079
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser504Ala
CA346754002
NM_001281493.2:c.1510T>G