Canonical Allele Identifier: PA1139738861
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 922501
ClinVar RCV Id: RCV001182613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val1866Phe
CA382546209
NM_001351834.2:c.5596G>T