Canonical Allele Identifier: PA658670101
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453651
ClinVar RCV Id: RCV001025812 RCV000524990 RCV003470680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser2310Asn
CA382557159
NM_000051.4:c.6929G>A