Canonical Allele Identifier: PA2825033269
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2175460
ClinVar RCV Id: RCV002602341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.His1474Gln
CA382532264
NM_000051.4:c.4422C>A
CA382532265
NM_000051.4:c.4422C>G