Allele Registry

Canonical Allele Identifier: PA346986

Gene: SLC52A3 HGNC NCBI

ClinVar RCV:

RCV000191966

ClinVar Variation:

210021

HGVS (amino-acid)	Matching Registered Transcripts
NP_212134.3:p.Ala312Val	CA346985 NM_033409.4:c.935C>T