Canonical Allele Identifier: PA2828492721
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 347545
ClinVar RCV Id: RCV000372817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358520.1:p.Leu13Val
CA10620097
NM_001371591.1:c.37C>G