Canonical Allele Identifier: PA2828088868
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 162380
ClinVar RCV Id: RCV000149774 RCV000149775
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350450.1:p.Asp263His
CA175008
NM_001363521.2:c.787G>C