Canonical Allele Identifier: PA171223
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 157839
ClinVar RCV Id: RCV000145150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ala1877Ser
CA171222
NM_018136.5:c.5629G>T