Allele Registry

Canonical Allele Identifier: PA2829197049

Gene: CRTAP HGNC NCBI

ClinVar RCV:

RCV000263295

RCV002518097

ClinVar Variation:

289670

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