Canonical Allele Identifier: PA1139727842
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 860092
ClinVar RCV Id: RCV001066337
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser2329Thr
CA382557786
NM_001351834.2:c.6986G>C