Allele Registry

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Canonical Allele Identifier: PA2826287326

Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 157786

ClinVar RCV Id: RCV000145088 RCV000594261

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001193775.1:p.Ser580Arg	CA271009 NM_001206846.2:c.1740C>G CA344013607 NM_001206846.2:c.1740C>A CA344013618 NM_001206846.2:c.1738A>C