Canonical Allele Identifier: PA2825035831
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1369427
ClinVar RCV Id: RCV001870624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp2625Gly
CA382561419
NM_000051.4:c.7874A>G