Canonical Allele Identifier: PA2826635659
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525821
ClinVar RCV Id: RCV000630151 RCV000776862
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ala381Gly
CA346750757
NM_001281494.2:c.1142C>G