Canonical Allele Identifier: PA315963
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 206150
ClinVar RCV Id: RCV000188168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689991.1:p.Asn148Asp
CA315962
NM_152778.4:c.442A>G