ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2829197491
Gene: CRTAP
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
452331
ClinVar RCV:
RCV000540867
ClinVar Variation:
465814
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001380293.1:p.Gly219Ser
CA2300355
NM_001393364.1:c.655G>A