Canonical Allele Identifier: PA2741866510
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2587822
ClinVar RCV Id: RCV003350801
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln876His
CA382544301
NM_001351834.2:c.2628A>C
CA382544304
NM_001351834.2:c.2628A>T