Allele Registry

Canonical Allele Identifier: PA2573317553

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV002012363

ClinVar Variation:

1492206

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.His453Tyr	CA3162841 NM_207352.4:c.1357C>T