Canonical Allele Identifier: PA2826635548
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 921312
ClinVar RCV Id: RCV001180660
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys358Arg
CA346750621
NM_001281494.2:c.1073A>G