Canonical Allele Identifier: PA2826287534
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2439256
ClinVar RCV Id: RCV003141591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Lys1129Asn
CA1310195
NM_001206846.2:c.3387A>T
CA344041443
NM_001206846.2:c.3387A>C