Canonical Allele Identifier: PA101491
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1005
ClinVar RCV Id: RCV000001060 RCV002222334 RCV002496222 RCV003137482 RCV002316184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689991.1:p.Pro412Leu
CA251664
NM_152778.4:c.1235C>T