Canonical Allele Identifier: PA916034844
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 490737
ClinVar RCV Id: RCV000582030 RCV000805253 RCV002221560 RCV002280130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg2849Pro
CA382518439
NM_001351834.2:c.8546G>C