Allele Registry

Canonical Allele Identifier: PA2828088933

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV000001057

ClinVar Variation:

1002

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350450.1:p.Gly324Asp	CA251660 NM_001363521.2:c.971G>A