Canonical Allele Identifier: PA2825031942
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1303049
ClinVar RCV Id: RCV001756548 RCV003107840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Pro884Ser
CA382545022
NM_000051.4:c.2650C>T