Canonical Allele Identifier: PA916033556
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 628138
ClinVar RCV Id: RCV000772451 RCV001856017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly1868Arg
CA382546241
NM_001351834.2:c.5602G>C
CA382546243
NM_001351834.2:c.5602G>A