Canonical Allele Identifier: PA2828492543
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 347542
ClinVar RCV Id: RCV000412876 RCV000544218 RCV001828342 RCV002487529
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358519.1:p.Leu324Phe
CA3077283
NM_001371590.1:c.972G>C
CA358171529
NM_001371590.1:c.972G>T