Canonical Allele Identifier: PA1139736955
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 876030
ClinVar RCV Id: RCV001100410
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ser317Arg
CA344018286
NM_018136.5:c.951T>A
CA344018288
NM_018136.5:c.951T>G
CA344018302
NM_018136.5:c.949A>C