Canonical Allele Identifier: PA2573078830
Gene: MTTP HGNC NCBI

Linked Data

ClinVar Variation Id: 14241
ClinVar RCV Id: RCV000015309
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373069.1:p.Ser590Ile
CA123822
NM_001386140.1:c.1769G>T