Canonical Allele Identifier: PA315970
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 206153
ClinVar RCV Id: RCV000188172 RCV000823577 RCV000765753 RCV002311276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689991.1:p.Ile226Thr
CA315969
NM_152778.4:c.677T>C