Canonical Allele Identifier: PA916033749
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 826159
ClinVar RCV Id: RCV001024843 RCV001862304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Tyr2019His
CA382550008
NM_001351834.2:c.6055T>C