Canonical Allele Identifier: PA1139737554
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 847462
ClinVar RCV Id: RCV001051010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val1446Ile
CA382531931
NM_001351834.2:c.4336G>A