Canonical Allele Identifier: PA2826705520
Gene: MFSD2A HGNC NCBI

Linked Data

ClinVar Variation Id: 372261
ClinVar RCV Id: RCV000412624 RCV002524634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274737.1:p.Ser10Leu
CA16042267
NM_001287808.2:c.29C>T