Canonical Allele Identifier: PA2580204764
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2097444
ClinVar RCV Id: RCV003018816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp1853Ser
CA2580083387
NM_001351834.2:c.5557_5558delinsAG