Canonical Allele Identifier: PA2829197547
Gene: CRTAP HGNC NCBI

Linked Data

ClinVar Variation Id: 4951
ClinVar RCV Id: RCV000005239 RCV002468961
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380294.1:p.Met1Ile