Canonical Allele Identifier: PA193163
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 185852
ClinVar RCV Id: RCV000165350 RCV000197653
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile671Lys
CA193161
NM_000051.4:c.2012T>A