Canonical Allele Identifier: PA2573203422
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1479672
ClinVar RCV Id: RCV002009862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Tyr2019Ser
CA382550013
NM_001351834.2:c.6056A>C