Canonical Allele Identifier: PA2830293979
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1440764
ClinVar RCV Id: RCV001978939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689991.1:p.Gly358Arg
CA3077302
NM_152778.4:c.1072G>A
CA358171774
NM_152778.4:c.1072G>C