Canonical Allele Identifier: PA2828442639
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 418295
ClinVar RCV Id: RCV000480079 RCV000505013 RCV000505174 RCV000504782 RCV000805545 RCV001542748 RCV002313243 RCV001805096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358523.1:p.Met405Thr
CA3077232
NM_001371594.1:c.1214T>C