Canonical Allele Identifier: PA2828443020
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 206150
ClinVar RCV Id: RCV000188168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358524.1:p.Asn103Asp
CA315962
NM_001371595.1:c.307A>G