Canonical Allele Identifier: PA658670534
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481211
ClinVar RCV Id: RCV000574916 RCV002526813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala2602Thr
CA382561267
NM_000051.4:c.7804G>A