Canonical Allele Identifier: PA2825035862
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2859728
ClinVar RCV Id: RCV003605400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr2640Pro
CA382561512
NM_000051.4:c.7918A>C