Canonical Allele Identifier: PA916033707
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 142164
ClinVar RCV Id: RCV000131129 RCV000484990 RCV001035231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu1991Asp
CA167651
NM_001351834.2:c.5973A>C
CA382548740
NM_001351834.2:c.5973A>T