Canonical Allele Identifier: PA2826625382
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 421018
ClinVar RCV Id: RCV000485837 RCV000582356 RCV000629703 RCV003464014 RCV004003341
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asp227Asn
CA067106
NM_001281492.2:c.679G>A