Canonical Allele Identifier: PA2829197491
Gene: CRTAP HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380293.1:p.Gly219Ser
CA2300355
NM_001393364.1:c.655G>A