Canonical Allele Identifier: PA645501138
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407609
ClinVar RCV Id: RCV000474745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser854Pro
CA16613107
NM_000051.4:c.2560T>C