Canonical Allele Identifier: PA060750
Gene: TTC7A HGNC NCBI

Linked Data

ClinVar Variation Id: 242605

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275882.1:p.Ser638Pro
CA060745
NM_001288953.2:c.1912T>C