Canonical Allele Identifier: PA2825034702
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1753082
ClinVar RCV Id: RCV002369056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser2123Asn
CA382553225
NM_000051.4:c.6368G>A