Canonical Allele Identifier: PA271105
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 157875
ClinVar RCV Id: RCV000145192 RCV000624327 RCV000710646 RCV001252170 RCV003905252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ser2557Cys
CA271104
NM_018136.5:c.7670C>G