Canonical Allele Identifier: PA2828441314
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2120001
ClinVar RCV Id: RCV003059164
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358522.1:p.Ala379Thr
CA358171172
NM_001371593.1:c.1135G>A