Canonical Allele Identifier: PA2828441177
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1914627
ClinVar RCV Id: RCV002597697
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358522.1:p.Val309Ile
CA358171951
NM_001371593.1:c.925G>A