Canonical Allele Identifier: PA2825032077
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1312663

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.His943Gln
CA382545819
NM_000051.4:c.2829C>A
CA382545821
NM_000051.4:c.2829C>G