Canonical Allele Identifier: PA2573203040
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1491253
ClinVar RCV Id: RCV001986393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp1803Val
CA382543791
NM_001351834.2:c.5408A>T