Canonical Allele Identifier: PA2741867150
Gene: ATM HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp1853Gly
CA382546022
NM_001351834.2:c.5558A>G