Canonical Allele Identifier: PA2573271803
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1444355
ClinVar RCV Id: RCV001982365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Leu1085Val
CA35884232
NM_018136.5:c.3253C>G