Canonical Allele Identifier: PA2826287234
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 876030
ClinVar RCV Id: RCV001100410

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193775.1:p.Ser317Arg
CA344018286
NM_001206846.2:c.951T>A
CA344018288
NM_001206846.2:c.951T>G
CA344018302
NM_001206846.2:c.949A>C