Canonical Allele Identifier: PA916031881
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453380
ClinVar RCV Id: RCV000545460 RCV000565682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu574Asp
CA382535284
NM_001351834.2:c.1722A>C
CA382535285
NM_001351834.2:c.1722A>T