Canonical Allele Identifier: PA2828088870
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 347542
ClinVar RCV Id: RCV000412876 RCV000544218 RCV001828342 RCV002487529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350450.1:p.Leu264Phe
CA3077283
NM_001363521.2:c.792G>C
CA358171529
NM_001363521.2:c.792G>T