Canonical Allele Identifier: PA916034219
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 231834
ClinVar RCV Id: RCV000220079 RCV000477984 RCV000557855 RCV003469041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala2386Pro
CA10579251
NM_001351834.2:c.7156G>C