Canonical Allele Identifier: PA916033279
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407499
ClinVar RCV Id: RCV000571141 RCV000456711 RCV002473013 RCV003230499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp1637Gly
CA6265583
NM_001351834.2:c.4910A>G