Canonical Allele Identifier: PA2573272071
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1658405
ClinVar RCV Id: RCV002175899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Arg2665Cys
CA1309304
NM_018136.5:c.7993C>T