Canonical Allele Identifier: PA913191707
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 628450
ClinVar RCV Id: RCV000772919 RCV001797140 RCV001067277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val1866Ile
CA382546205
NM_000051.4:c.5596G>A