Canonical Allele Identifier: PA2828441203
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2415035
ClinVar RCV Id: RCV003110454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358522.1:p.Gln327Arg
CA358171653
NM_001371593.1:c.980A>G