Canonical Allele Identifier: PA916031614
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482557
ClinVar RCV Id: RCV000573582 RCV001858236
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu364Ser
CA382532363
NM_001351834.2:c.1091T>C