Canonical Allele Identifier: PA2828493068
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1440764
ClinVar RCV Id: RCV001978939
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358520.1:p.Gly358Arg
CA3077302
NM_001371591.1:c.1072G>A
CA358171774
NM_001371591.1:c.1072G>C