Canonical Allele Identifier: PA2825033999
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_000042.3:p.Asp1803Val
CA382543791
NM_000051.4:c.5408A>T