Canonical Allele Identifier: PA2828493119
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1446647

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358520.1:p.Tyr410His
CA3077264
NM_001371591.1:c.1228T>C