Canonical Allele Identifier: PA2580220047
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2182967
ClinVar RCV Id: RCV002592289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358521.1:p.Met393Thr
CA358171338
NM_001371592.1:c.1178T>C