Canonical Allele Identifier: PA2828088913
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 950479
ClinVar RCV Id: RCV001222197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350450.1:p.Pro307Gly
CA1139658218
NM_001363521.2:c.919_920delinsGG