Canonical Allele Identifier: PA2580199999
Gene: TTC7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2189338
ClinVar RCV Id: RCV002636773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275880.1:p.Val857Ile
CA346718054
NM_001288951.2:c.2569G>A