Canonical Allele Identifier: PA916032082
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453405
ClinVar RCV Id: RCV000527386 RCV001805139
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val723Leu
CA382538784
NM_001351834.2:c.2167G>C
CA382538786
NM_001351834.2:c.2167G>T