Canonical Allele Identifier: PA916062766
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 672229
ClinVar RCV Id: RCV000831460 RCV004029212
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Arg2202Ser
CA1309561
NM_018136.5:c.6606A>T
CA344022448
NM_018136.5:c.6606A>C