Canonical Allele Identifier: PA2828440988
Gene: MFSD8 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358522.1:p.Leu194Arg
CA358175309
NM_001371593.1:c.581T>G