Canonical Allele Identifier: PA2828088710
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 934468
ClinVar RCV Id: RCV001202866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350450.1:p.Tyr121Ser
CA3077495
NM_001363521.2:c.362A>C