Canonical Allele Identifier: PA2826634872
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1774324
ClinVar RCV Id: RCV002392326
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp204Asn
CA346746337
NM_001281494.2:c.610G>A