Canonical Allele Identifier: PA199690
Gene: TTC7A HGNC NCBI

Linked Data

ClinVar Variation Id: 190395

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275882.1:p.Glu37Lys
CA199689
NM_001288953.2:c.109G>A