Canonical Allele Identifier: PA916034021
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481331
ClinVar RCV Id: RCV000572457 RCV002530246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Pro2222His
CA382554855
NM_001351834.2:c.6665C>A