Canonical Allele Identifier: PA2828443477
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1756403
ClinVar RCV Id: RCV002378178
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358524.1:p.Pro318Ser
CA358171201
NM_001371595.1:c.952C>T