Canonical Allele Identifier: PA2828088951
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 418295
ClinVar RCV Id: RCV000480079 RCV000505013 RCV000505174 RCV000504782 RCV000805545 RCV001542748 RCV002313243 RCV001805096
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350450.1:p.Met349Thr
CA3077232
NM_001363521.2:c.1046T>C