Canonical Allele Identifier: PA891845000
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 567934
ClinVar RCV Id: RCV000688146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val725Asp
CA382538811
NM_000051.4:c.2174T>A