Canonical Allele Identifier: PA2825035852
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 922945
ClinVar RCV Id: RCV001183307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala2635Asp
CA6266208
NM_000051.4:c.7904C>A