Canonical Allele Identifier: PA2580420942
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2439256
ClinVar RCV Id: RCV003141591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Lys1129Asn
CA1310195
NM_018136.5:c.3387A>T
CA344041443
NM_018136.5:c.3387A>C