Canonical Allele Identifier: PA645408418
Gene: MFSD2A HGNC NCBI

Linked Data

ClinVar Variation Id: 372261

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129965.1:p.Ser179Leu
CA16042267
NM_001136493.3:c.536C>T