Canonical Allele Identifier: PA916017119
Gene: TTC7A HGNC NCBI

Linked Data

ClinVar Variation Id: 190394
ClinVar RCV Id: RCV000170532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275880.1:p.Ala856Thr
CA10575707
NM_001288951.2:c.2566G>A