Canonical Allele Identifier: PA658669549
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453579
ClinVar RCV Id: RCV000557051
ClinVar Variation Id: 2125329
ClinVar RCV Id: RCV003040057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp1815Glu
CA382544184
NM_000051.4:c.5445C>A
CA382544186
NM_000051.4:c.5445C>G