Canonical Allele Identifier: PA2826287230
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 210363
ClinVar RCV Id: RCV000192474 RCV000710651 RCV000714630 RCV004020311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Ser311Arg
CA205314
NM_001206846.2:c.933C>G
CA344018382
NM_001206846.2:c.933C>A
CA344018392
NM_001206846.2:c.931A>C