Canonical Allele Identifier: PA916031553
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 567449
ClinVar RCV Id: RCV000687539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.His325Leu
CA382531093
NM_001351834.2:c.974A>T