Canonical Allele Identifier: PA2826747882
Gene: TTC7A HGNC NCBI

Linked Data

ClinVar Variation Id: 50609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275884.1:p.Leu469Pro
CA143779
NM_001288955.2:c.1406T>C