Canonical Allele Identifier: PA658739150
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 490476
ClinVar RCV Id: RCV000584604 RCV001320169
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn856Ser
CA382543835
NM_000051.4:c.2567A>G