Canonical Allele Identifier: PA645479857
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 347545
ClinVar RCV Id: RCV000372817
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689991.1:p.Leu13Val
CA10620097
NM_152778.4:c.37C>G