Canonical Allele Identifier: PA2825827074
Gene: MFSD2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2241768
ClinVar RCV Id: RCV002767273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129965.1:p.Ala180Val
CA339834762
NM_001136493.3:c.539C>T