Canonical Allele Identifier: PA2741866496
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2587762
ClinVar RCV Id: RCV003360984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asn856Ile
CA382543838
NM_001351834.2:c.2567A>T