Canonical Allele Identifier: PA2826746435
Gene: TTC7A HGNC NCBI
ClinVar RCV:
RCV001325687
ClinVar Variation:
1025381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275880.1:p.Tyr10Phe
CA346715555
NM_001288951.2:c.29A>T