Canonical Allele Identifier: PA2825033720
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3221687
ClinVar RCV Id: RCV004511011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Pro1680Ser
CA382540336
NM_000051.4:c.5038C>T