Allele Registry

Canonical Allele Identifier: PA101537

Gene: MFSD8 HGNC NCBI

ClinVar Allele:

16045

ClinVar RCV:

RCV000001061

RCV001781155

RCV001826401

RCV002371752

ClinVar Variation:

1006

HGVS (amino-acid)	Matching Registered Transcripts
NP_689991.1:p.Thr294Lys	CA339858 NM_152778.4:c.881C>A