Canonical Allele Identifier: PA2826705710
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_001274738.1:p.Ser129Leu
CA16042267
NM_001287809.2:c.386C>T