Canonical Allele Identifier: PA645443995
Gene: MTTP HGNC NCBI

Linked Data

ClinVar Variation Id: 347021
ClinVar RCV Id: RCV000276357 RCV001192652 RCV001522721
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000244.2:p.Glu98Asp
CA3021799
NM_000253.4:c.294G>C
CA102617498
NM_000253.4:c.294G>T