Canonical Allele Identifier: PA1139764490
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 838564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689991.1:p.Ile181Val
CA358176034
NM_152778.4:c.541A>G