Canonical Allele Identifier: PA2828444275
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2153369
ClinVar RCV Id: RCV003085627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358525.1:p.Asn171Lys
CA358176181
NM_001371596.2:c.513C>G
CA358176182
NM_001371596.2:c.513C>A