Canonical Allele Identifier: PA2828088490
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1451070
ClinVar RCV Id: RCV001993086
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350449.1:p.Met369Thr
CA358170996
NM_001363520.2:c.1106T>C