Canonical Allele Identifier: PA095782
Gene: MTTP HGNC NCBI

Linked Data

ClinVar Variation Id: 14240
ClinVar RCV Id: RCV000015308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000244.2:p.Asn780Tyr
CA123821
NM_000253.4:c.2338A>T