Canonical Allele Identifier: PA1139764491
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 967674
ClinVar RCV Id: RCV001242649
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689991.1:p.Val185Leu
CA358175984
NM_152778.4:c.553G>C