Allele Registry

Canonical Allele Identifier: PA107390

Gene: PCCA HGNC NCBI

ClinVar Allele:

47473

ClinVar RCV:

RCV000032111

ClinVar Variation:

38868

HGVS (amino-acid)	Matching Registered Transcripts
NP_000273.2:p.Ile164Thr	CA343124 NM_000282.4:c.491T>C