Canonical Allele Identifier: PA207955
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 211495
ClinVar RCV Id: RCV000194054 RCV000662085 RCV002517099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689991.1:p.Ile312Thr
CA207954
NM_152778.4:c.935T>C