Canonical Allele Identifier: PA168128
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 142345
ClinVar RCV Id: RCV000131419 RCV000168043 RCV000484154 RCV000779790 RCV001762310
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile826Leu
CA168126
NM_000051.4:c.2476A>C