Canonical Allele Identifier: PA2826635964
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr455Asn
CA346752822
NM_001281494.2:c.1364C>A