Canonical Allele Identifier: PA2826287526
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 585444
ClinVar RCV Id: RCV000710630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Tyr1109Cys
CA344041862
NM_001206846.2:c.3326A>G