Canonical Allele Identifier: PA2741866852
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2754315
ClinVar RCV Id: RCV003500086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp1367Glu
CA382528602
NM_001351834.2:c.4101C>A
CA382528604
NM_001351834.2:c.4101C>G