Canonical Allele Identifier: PA2828441300
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1446647

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358522.1:p.Tyr372His
CA3077264
NM_001371593.1:c.1114T>C