Canonical Allele Identifier: PA916034719
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 186351
ClinVar RCV Id: RCV000165932 RCV000200060 RCV003468762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly2765Ser
CA194563
NM_001351834.2:c.8293G>A