Canonical Allele Identifier: PA315949
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_689991.1:p.Pro69Leu
CA315948
NM_152778.4:c.206C>T