Allele Registry

Canonical Allele Identifier: PA2826131918

Gene: PCCA HGNC NCBI

ClinVar Allele:

214900

ClinVar RCV:

RCV000236842

ClinVar Variation:

218253

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171475.1:p.Cys641Arg	CA7033896 NM_001178004.2:c.1921T>C