Canonical Allele Identifier: PA645395098
Gene: ASPM HGNC NCBI
ClinVar RCV:
RCV000285661
ClinVar Variation:
294614
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Arg2281Ser
CA1309507
NM_018136.5:c.6843A>T
CA344021273
NM_018136.5:c.6843A>C