Canonical Allele Identifier: PA2828493129
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1432417
ClinVar RCV Id: RCV001941251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358520.1:p.Leu420Phe
CA358171150
NM_001371591.1:c.1258C>T