Canonical Allele Identifier: PA2825034485
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 951342
ClinVar RCV Id: RCV001223230
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg2032Ile
CA382550221
NM_000051.4:c.6095G>T