Canonical Allele Identifier: PA2573271992
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 1390578
ClinVar RCV Id: RCV001891068 RCV003452066
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.Phe2127Leu
CA35871367
NM_018136.5:c.6381T>A
CA344023034
NM_018136.5:c.6381T>G
CA344023038
NM_018136.5:c.6379T>C