Canonical Allele Identifier: PA916032030
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 221183
ClinVar RCV Id: RCV000204655 RCV001785517 RCV004020549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln684His
CA348859
NM_001351834.2:c.2052G>C
CA382537455
NM_001351834.2:c.2052G>T