Canonical Allele Identifier: PA2828441358
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1002
ClinVar RCV Id: RCV000001057
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358522.1:p.Gly391Asp
CA251660
NM_001371593.1:c.1172G>A