Canonical Allele Identifier: PA2828441307
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1005
ClinVar RCV Id: RCV000001060 RCV002222334 RCV002496222 RCV003137482 RCV002316184
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358522.1:p.Pro374Leu
CA251664
NM_001371593.1:c.1121C>T