Canonical Allele Identifier: PA891845122
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 584489
ClinVar RCV Id: RCV000708651 RCV003605673
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala1359Asp
CA382528267
NM_000051.4:c.4076C>A