Canonical Allele Identifier: PA2828493037
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 533373
ClinVar RCV Id: RCV000640467 RCV001835890
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358520.1:p.Lys333Asn
CA358172133
NM_001371591.1:c.999G>T
CA358172136
NM_001371591.1:c.999G>C