Canonical Allele Identifier: PA2828492896
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 967674
ClinVar RCV Id: RCV001242649
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358520.1:p.Val185Leu
CA358175984
NM_001371591.1:c.553G>C