Canonical Allele Identifier: PA2825031547
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1406359
ClinVar RCV Id: RCV001915785
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile709Asn
CA382538635
NM_000051.4:c.2126T>A