Canonical Allele Identifier: PA2828442449
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_001358523.1:p.Gly309Arg
CA3077302
NM_001371594.1:c.925G>A
CA358171774
NM_001371594.1:c.925G>C