Canonical Allele Identifier: PA916033920
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481276
ClinVar RCV Id: RCV000568862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu2126Lys
CA382553265
NM_001351834.2:c.6376G>A