Canonical Allele Identifier: PA2826849234
Gene: MTTP HGNC NCBI

Linked Data

ClinVar Variation Id: 1412047
ClinVar RCV Id: RCV001918980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287714.2:p.Arg326Ile
CA357508672
NM_001300785.2:c.977G>T
CA2573138379
NM_001300785.2:c.977_978delinsTT