Canonical Allele Identifier: PA2828444420
Gene: MFSD8 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358525.1:p.Leu232Arg
CA358175309
NM_001371596.2:c.695T>G