Canonical Allele Identifier: PA2826747719
Gene: TTC7A HGNC NCBI

Linked Data

ClinVar Variation Id: 242606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275884.1:p.Lys252Arg
CA060659
NM_001288955.2:c.755A>G