Canonical Allele Identifier: PA2828443329
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 162380
ClinVar RCV Id: RCV000149774 RCV000149775
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358524.1:p.Asp274His
CA175008
NM_001371595.1:c.820G>C