Canonical Allele Identifier: PA2828492293
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 934468
ClinVar RCV Id: RCV001202866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358519.1:p.Tyr76Ser
CA3077495
NM_001371590.1:c.227A>C