Canonical Allele Identifier: PA2828088687
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 206140
ClinVar RCV Id: RCV000188156 RCV001857624
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350450.1:p.Ile93Val
CA315943
NM_001363521.2:c.277A>G