Allele Registry

Canonical Allele Identifier: PA2828088600

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV000372817

ClinVar Variation:

347545

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350450.1:p.Leu13Val	CA10620097 NM_001363521.2:c.37C>G