Canonical Allele Identifier: PA2573072382
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 211495
ClinVar RCV Id: RCV000194054 RCV000662085 RCV002517099
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358521.1:p.Ile314Thr
CA207954
NM_001371592.1:c.941T>C