Canonical Allele Identifier: PA2826635989
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 619576
ClinVar RCV Id: RCV000758667
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp461Asn
CA346752932
NM_001281494.2:c.1381G>A