Canonical Allele Identifier: PA1139693873
Gene: TTC7A HGNC NCBI

Linked Data

ClinVar Variation Id: 935737
ClinVar RCV Id: RCV001204390
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275880.1:p.Ile878Val
CA1648198
NM_001288951.2:c.2632A>G