Canonical Allele Identifier: PA2825031461
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1379534
ClinVar RCV Id: RCV001883823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile671Met
CA382537090
NM_000051.4:c.2013A>G