Canonical Allele Identifier: PA658673870
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453397
ClinVar RCV Id: RCV000543713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp658Glu
CA382536846
NM_000051.4:c.1974C>A
CA382536849
NM_000051.4:c.1974C>G