Canonical Allele Identifier: PA2826586790
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1736032
ClinVar RCV Id: RCV002373095
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asn999Ile
CA346761426
NM_001281494.2:c.2996A>T