Canonical Allele Identifier: PA2499251021
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1062781
ClinVar RCV Id: RCV001372537
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu1861Met
CA382546133
NM_001351834.2:c.5581C>A