Canonical Allele Identifier: PA2828443997
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 206143
ClinVar RCV Id: RCV001086515 RCV000725884 RCV002317122
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358525.1:p.Pro69Leu
CA315948
NM_001371596.2:c.206C>T