Canonical Allele Identifier: PA916033538
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 572732
ClinVar RCV Id: RCV000694184 RCV002343483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asn1855Lys
CA382546051
NM_001351834.2:c.5565T>A
CA382546053
NM_001351834.2:c.5565T>G