Canonical Allele Identifier: PA2826627058
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455183

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asn621Ile
CA346752673
NM_001281492.2:c.1862A>T