Canonical Allele Identifier: PA101537
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1006
ClinVar RCV Id: RCV000001061 RCV001826401 RCV001781155 RCV002371752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689991.1:p.Thr294Lys
CA339858
NM_152778.4:c.881C>A