Canonical Allele Identifier: PA2826849230
Gene: MTTP HGNC NCBI

Linked Data

ClinVar Variation Id: 2193516
ClinVar RCV Id: RCV002623981
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287714.2:p.Asn321Ser
CA3022047
NM_001300785.2:c.962A>G