Canonical Allele Identifier: PA2825030696
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 645300
ClinVar RCV Id: RCV000799355 RCV001009667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly335Glu
CA382531377
NM_000051.4:c.1004G>A