Canonical Allele Identifier: PA658801836
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 524341
ClinVar RCV Id: RCV000628054 RCV001766332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala2225Thr
CA382554870
NM_000051.4:c.6673G>A