Allele Registry

Canonical Allele Identifier: PA2828440740

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV000372817

ClinVar Variation:

347545

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358522.1:p.Leu13Val	CA10620097 NM_001371593.1:c.37C>G