Canonical Allele Identifier: PA2741866107
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2642356
ClinVar RCV Id: RCV003396066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asn567His
CA382535234
NM_001351834.2:c.1699A>C