Canonical Allele Identifier: PA916031728
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453359
ClinVar RCV Id: RCV000526412 RCV000582808 RCV003470664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly449Glu
CA382533760
NM_001351834.2:c.1346G>A