Canonical Allele Identifier: PA171235
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 157857
ClinVar RCV Id: RCV000145170 RCV000224688 RCV001099997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Val2243Leu
CA171234
NM_018136.5:c.6727G>T
CA344021651
NM_018136.5:c.6727G>C