Allele Registry

Canonical Allele Identifier: PA2573317540

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV001893064

ClinVar Variation:

1391408

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Thr417Ser	CA3162810 NM_207352.4:c.1249A>T CA358950389 NM_207352.4:c.1250C>G