Canonical Allele Identifier: PA916034553
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 234050
ClinVar RCV Id: RCV000221138 RCV003469096 RCV002516176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly2644Ser
CA10579276
NM_001351834.2:c.7930G>A