Canonical Allele Identifier: PA171221
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 157838
ClinVar RCV Id: RCV000145149 RCV000322632 RCV000965579
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Ala1877Thr
CA171220
NM_018136.5:c.5629G>A