Canonical Allele Identifier: PA2580205681
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2159509
ClinVar RCV Id: RCV003087395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala2225Ser
CA382554872
NM_001351834.2:c.6673G>T