Canonical Allele Identifier: PA2825078001
Gene: MTTP HGNC NCBI

Linked Data

ClinVar Variation Id: 1416980
ClinVar RCV Id: RCV001923477
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000244.2:p.His871Tyr
CA3022414
NM_000253.4:c.2611C>T