Canonical Allele Identifier: PA2825034523
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 641310
ClinVar RCV Id: RCV000794523

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val2047dup
CA915947651
NM_000051.4:c.6139_6141dup