Canonical Allele Identifier: PA2828492402
Gene: MFSD8 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358519.1:p.Leu187Arg
CA358175309
NM_001371590.1:c.560T>G