Canonical Allele Identifier: PA2828441270
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2420398
ClinVar RCV Id: RCV003121563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358522.1:p.Thr361Ile
CA358171282
NM_001371593.1:c.1082C>T