Canonical Allele Identifier: PA2580219953
Gene: MFSD8 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358521.1:p.Leu234Arg
CA358175309
NM_001371592.1:c.701T>G