Canonical Allele Identifier: PA2499286150
Gene: TTC7A HGNC NCBI
ClinVar RCV:
RCV001325687
ClinVar Variation:
1025381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065191.2:p.Tyr10Phe
CA346715555
NM_020458.3:c.29A>T