Canonical Allele Identifier: PA2825035400
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1023012
ClinVar RCV Id: RCV001322998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg2428Lys
CA382559789
NM_000051.4:c.7283G>A