Canonical Allele Identifier: PA916031997
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 642029
ClinVar RCV Id: RCV000795417 RCV002422702 RCV003467347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp658Asn
CA382536833
NM_001351834.2:c.1972G>A