Canonical Allele Identifier: PA2830294157
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 950479
ClinVar RCV Id: RCV001222197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689991.1:p.Pro412Gly
CA1139658218
NM_152778.4:c.1234_1235delinsGG