Canonical Allele Identifier: PA645480073
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 347542

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689991.1:p.Leu369Phe
CA3077283
NM_152778.4:c.1107G>C
CA358171529
NM_152778.4:c.1107G>T