Canonical Allele Identifier: PA2828492990
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1006
ClinVar RCV Id: RCV000001061 RCV001826401 RCV001781155 RCV002371752
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358520.1:p.Thr294Lys
CA339858
NM_001371591.1:c.881C>A