Canonical Allele Identifier: PA2741867310
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2993095
ClinVar RCV Id: RCV003850190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Tyr2049His
CA382550545
NM_001351834.2:c.6145T>C