Canonical Allele Identifier: PA2829197049
Gene: CRTAP HGNC NCBI

Linked Data

ClinVar Variation Id: 289670
ClinVar RCV Id: RCV000263295 RCV002518097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380292.1:p.Gly7Ala
CA10606514
NM_001393363.1:c.20G>C