Canonical Allele Identifier: PA2825034928
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1754752
ClinVar RCV Id: RCV002366914 RCV003607476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Pro2222Leu
CA382554856
NM_000051.4:c.6665C>T