Canonical Allele Identifier: PA2825034253
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 924050
ClinVar RCV Id: RCV001185171 RCV001876170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly1925Ala
CA382548295
NM_000051.4:c.5774G>C