Canonical Allele Identifier: PA2828493018
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_001358520.1:p.Ile312Thr
CA207954
NM_001371591.1:c.935T>C