Allele Registry

Canonical Allele Identifier: PA2826954986

Gene: PRKCD HGNC NCBI

ClinVar Allele:

1004924

ClinVar RCV:

RCV001320243

ClinVar Variation:

1020633

HGVS (amino-acid)	Matching Registered Transcripts
NP_001303256.1:p.Ala212Val	CA2451901 NM_001316327.2:c.635C>T