Canonical Allele Identifier: PA2828443529
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1026836
ClinVar RCV Id: RCV001327341 RCV001830386
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358524.1:p.Ser343Tyr
CA358170980
NM_001371595.1:c.1028C>A