Canonical Allele Identifier: PA2573072363
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 206153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358521.1:p.Ile228Thr
CA315969
NM_001371592.1:c.683T>C