Canonical Allele Identifier: PA2580204749
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2453929
ClinVar RCV Id: RCV003188064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val1841Leu
CA382545801
NM_001351834.2:c.5521G>C
CA382545804
NM_001351834.2:c.5521G>T