Canonical Allele Identifier: PA2825034122
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 841402
ClinVar RCV Id: RCV001043614 RCV002348363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu1862Val
CA382546149
NM_000051.4:c.5584C>G