Canonical Allele Identifier: PA645503851
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 232481
ClinVar RCV Id: RCV000222504 RCV000233636 RCV000486420 RCV000764945 RCV001818535 RCV003338468
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn2501Ser
CA6266116
NM_000051.4:c.7502A>G