Allele Registry

Canonical Allele Identifier: PA915985198

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV000670930

ClinVar Variation:

555164

HGVS (amino-acid)	Matching Registered Transcripts
NP_001458.1:p.Phe31Tyr	CA382908431 NM_001467.6:c.92T>A