Canonical Allele Identifier: PA2825077090
Gene: MTTP HGNC NCBI

Linked Data

ClinVar Variation Id: 2084455
ClinVar RCV Id: RCV002994717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000244.2:p.Val89Ala
CA102617438
NM_000253.4:c.266T>C