Canonical Allele Identifier: PA2580203410
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1792552
ClinVar RCV Id: RCV002433061 RCV003465761 RCV003500795
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp841Asn
CA382543479
NM_001351834.2:c.2521G>A