Canonical Allele Identifier: PA2828441387
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1770460
ClinVar RCV Id: RCV002387808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358522.1:p.Pro411Ser
CA105670616
NM_001371593.1:c.1231C>T