Allele Registry

Canonical Allele Identifier: PA2830293336

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV001202866

ClinVar Variation:

934468

HGVS (amino-acid)	Matching Registered Transcripts
NP_689991.1:p.Tyr121Ser	CA3077495 NM_152778.4:c.362A>C