Canonical Allele Identifier: PA2741866506
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2864737
ClinVar RCV Id: RCV003605492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asn870Tyr
CA382544144
NM_001351834.2:c.2608A>T