Canonical Allele Identifier: PA1139734398
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 935510
ClinVar RCV Id: RCV001204120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln654His
CA382536784
NM_001351834.2:c.1962G>C
CA382536785
NM_001351834.2:c.1962G>T