Canonical Allele Identifier: PA2828492890
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1707798
ClinVar RCV Id: RCV002286959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358520.1:p.Leu178Phe
CA358176066
NM_001371591.1:c.534A>T
CA358176069
NM_001371591.1:c.534A>C