Canonical Allele Identifier: PA891855704
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 585444
ClinVar RCV Id: RCV000710630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Tyr1109Cys
CA344041862
NM_018136.5:c.3326A>G