Canonical Allele Identifier: PA2828441151
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 162378
ClinVar RCV Id: RCV000149771 RCV001080724 RCV000732335 RCV001272733 RCV002509247 RCV002316957 RCV003917467
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358522.1:p.Glu298Gln
CA175005
NM_001371593.1:c.892G>C