Canonical Allele Identifier: PA2573204450
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1369409
ClinVar RCV Id: RCV001870612

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu726Val
CA382538820
NM_001351834.2:c.2176C>G