Canonical Allele Identifier: PA2825032446
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 653038
ClinVar RCV Id: RCV000808726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp1103Val
CA382517393
NM_000051.4:c.3308A>T