Canonical Allele Identifier: PA645504340
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 246331
ClinVar RCV Id: RCV000235760 RCV000562391 RCV000706089 RCV003993907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Pro2699Arg
CA10584370
NM_000051.4:c.8096C>G