Allele Registry

Canonical Allele Identifier: PA2825653719

Gene: PCCA HGNC NCBI

ClinVar Allele:

214887

ClinVar RCV:

RCV000235343

ClinVar Variation:

218248

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121164.1:p.Asp69Gly	CA10575823 NM_001127692.3:c.206A>G