Canonical Allele Identifier: PA2580206422
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2130896
ClinVar RCV Id: RCV003052316
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr2556Ser
CA382560963
NM_001351834.2:c.7666A>T
CA382560965
NM_001351834.2:c.7667C>G