Canonical Allele Identifier: PA2826287457
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1713844
ClinVar RCV Id: RCV002303129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Leu946Phe
CA344048919
NM_001206846.2:c.2838A>T
CA344048920
NM_001206846.2:c.2838A>C