Canonical Allele Identifier: PA2828443257
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_001358524.1:p.Lys239Asn
CA358172133
NM_001371595.1:c.717G>T
CA358172136
NM_001371595.1:c.717G>C