Canonical Allele Identifier: PA2573202027
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1519566
ClinVar RCV Id: RCV002024690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu1255Ser
CA382524341
NM_001351834.2:c.3764T>C