Canonical Allele Identifier: PA2828492396
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 206153
ClinVar RCV Id: RCV000188172 RCV000823577 RCV000765753 RCV002311276
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358519.1:p.Ile181Thr
CA315969
NM_001371590.1:c.542T>C