Canonical Allele Identifier: PA2825077998
Gene: MTTP HGNC NCBI

Linked Data

ClinVar Variation Id: 1354857
ClinVar RCV Id: RCV001887895

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000244.2:p.Pro869Leu
CA357520462
NM_000253.4:c.2606C>T
CA645520134
NM_000253.4:c.2606_2607delinsTT