Canonical Allele Identifier: PA2826636137
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1428818
ClinVar RCV Id: RCV001936488
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp495Asn
CA346753817
NM_001281494.2:c.1483G>A