Canonical Allele Identifier: PA916034542
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407514
ClinVar RCV Id: RCV000467501 RCV000569832
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Trp2638Cys
CA6266211
NM_001351834.2:c.7914G>T
CA382561504
NM_001351834.2:c.7914G>C