Canonical Allele Identifier: PA2830293635
Gene: MFSD8 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689991.1:p.Leu232Arg
CA358175309
NM_152778.4:c.695T>G