Canonical Allele Identifier: PA916033454
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 419933
ClinVar RCV Id: RCV000485627 RCV000582760 RCV000628045 RCV003230516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val1777Ile
CA16619197
NM_001351834.2:c.5329G>A