Canonical Allele Identifier: PA2828442029
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1007
ClinVar RCV Id: RCV000001062
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358523.1:p.Ala157Pro
CA358176397
NM_001371594.1:c.469G>C
CA1139658643
NM_001371594.1:c.468_469delinsCC