Canonical Allele Identifier: PA2828492506
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 162378
ClinVar RCV Id: RCV000149771 RCV001080724 RCV000732335 RCV001272733 RCV002509247 RCV002316957 RCV003917467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358519.1:p.Glu291Gln
CA175005
NM_001371590.1:c.871G>C