Allele Registry

Canonical Allele Identifier: PA2826726386

Gene: C2CD3 HGNC NCBI

ClinVar RCV:

RCV000418985

ClinVar Variation:

389647

HGVS (amino-acid)	Matching Registered Transcripts
NP_001273506.1:p.Asp1028Tyr	CA16606332 NM_001286577.2:c.3082G>T