Canonical Allele Identifier: PA2828493096
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2077803
ClinVar RCV Id: RCV002985707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358520.1:p.Trp387Cys
CA358171360
NM_001371591.1:c.1161G>T
CA358171362
NM_001371591.1:c.1161G>C