Canonical Allele Identifier: PA916032209
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407552
ClinVar RCV Id: RCV000467140 RCV001183457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp831Tyr
CA16613293
NM_001351834.2:c.2491G>T