Canonical Allele Identifier: PA2828441395
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 418295

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358522.1:p.Met416Thr
CA3077232
NM_001371593.1:c.1247T>C