Canonical Allele Identifier: PA916034351
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407715
ClinVar RCV Id: RCV000477084 RCV001026441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Met2482Val
CA16613428
NM_001351834.2:c.7444A>G