Allele Registry

Canonical Allele Identifier: PA2573072380

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV000001056

ClinVar Variation:

1001

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358521.1:p.Gly312Asp	CA251659 NM_001371592.1:c.935G>A