Canonical Allele Identifier: PA645498954
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 236798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg329Lys
CA6264714
NM_000051.4:c.986G>A