Allele Registry

Canonical Allele Identifier: PA3057574833

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV005200474

ClinVar Variation:

3720604

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Tyr343Asp	CA358949319 NM_207352.4:c.1027T>G