Canonical Allele Identifier: PA913191741
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 631410
ClinVar RCV Id: RCV000777620 RCV001036032 RCV003465703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile2275Thr
CA382556516
NM_000051.4:c.6824T>C