Canonical Allele Identifier: PA645395088
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 294617
ClinVar RCV Id: RCV000301005 RCV000991553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Asn2237Lys
CA10609236
NM_018136.5:c.6711C>A
CA344021684
NM_018136.5:c.6711C>G