Canonical Allele Identifier: PA2828442048
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2194111
ClinVar RCV Id: RCV002647330
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358523.1:p.Asn171Asp
CA358176191
NM_001371594.1:c.511A>G