Canonical Allele Identifier: PA2580421010
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2443510
ClinVar RCV Id: RCV003152117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.His1898Gln
CA344024750
NM_018136.5:c.5694T>G
CA344024752
NM_018136.5:c.5694T>A