Canonical Allele Identifier: PA197120
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 187235
ClinVar RCV Id: RCV000166950 RCV000801758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr547Ile
CA197118
NM_000051.4:c.1640C>T