Canonical Allele Identifier: PA2573203028
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1438719
ClinVar RCV Id: RCV001949047
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Pro1797Leu
CA382543623
NM_001351834.2:c.5390C>T