Canonical Allele Identifier: PA203527
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 198619
ClinVar RCV Id: RCV000180004 RCV000461551 RCV001273684 RCV001721127 RCV002314668 RCV003947538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689991.1:p.Gly197Asp
CA203526
NM_152778.4:c.590G>A