Canonical Allele Identifier: PA916033468
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481089
ClinVar RCV Id: RCV000574069 RCV000627950 RCV003321675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp1790Val
CA382543413
NM_001351834.2:c.5369A>T