Canonical Allele Identifier: PA658669839
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453610

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly2023Glu
CA382550080
NM_000051.4:c.6068G>A