Canonical Allele Identifier: PA143780
Gene: TTC7A HGNC NCBI

Linked Data

ClinVar Variation Id: 50609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275882.1:p.Leu789Pro
CA143779
NM_001288953.2:c.2366T>C