Canonical Allele Identifier: PA2573204802
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1511620
ClinVar RCV Id: RCV002016850
ClinVar Variation Id: 2816234
ClinVar RCV Id: RCV003606247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys940Asn
CA382545776
NM_001351834.2:c.2820A>C
CA382545779
NM_001351834.2:c.2820A>T