Canonical Allele Identifier: PA916033418
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407510
ClinVar RCV Id: RCV000465365 RCV000566161 RCV003985355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly1746Arg
CA16613442
NM_001351834.2:c.5236G>A
CA382542382
NM_001351834.2:c.5236G>C