Canonical Allele Identifier: PA2573271915
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1394619
ClinVar RCV Id: RCV001900946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Arg1695His
CA1309814
NM_018136.5:c.5084G>A