Canonical Allele Identifier: PA2580203343
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2086236
ClinVar RCV Id: RCV003007387

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala736Gly
CA382539025
NM_001351834.2:c.2207C>G