Canonical Allele Identifier: PA2499250979
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1049347
ClinVar RCV Id: RCV001355347 RCV002413839 RCV003605757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile2629Val
CA382561443
NM_001351834.2:c.7885A>G