Allele Registry

Canonical Allele Identifier: PA2827665001

Gene: PCCA HGNC NCBI

ClinVar RCV:

RCV000235343

ClinVar Variation:

218248

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339537.1:p.Asp69Gly	CA10575823 NM_001352608.2:c.206A>G