Canonical Allele Identifier: PA2580206619
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2109103
ClinVar RCV Id: RCV003038195
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp2650Gly
CA382561691
NM_001351834.2:c.7949A>G