Canonical Allele Identifier: PA2825033013
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2802714
ClinVar RCV Id: RCV003606074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser1358Cys
CA382528193
NM_000051.4:c.4072A>T