Canonical Allele Identifier: PA2825032829
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1721789
ClinVar RCV Id: RCV002302189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.His1264Pro
CA382524616
NM_000051.4:c.3791A>C