Canonical Allele Identifier: PA2825035833
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1760976
ClinVar RCV Id: RCV002412289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp2625Val
CA382561420
NM_000051.4:c.7874A>T