Canonical Allele Identifier: PA645504444
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp2708His
CA16613497
NM_000051.4:c.8122G>C