Canonical Allele Identifier: PA2828493084
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 853164
ClinVar RCV Id: RCV001057924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358520.1:p.Ile374Val
CA358171457
NM_001371591.1:c.1120A>G