Canonical Allele Identifier: PA916034507
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 584496
ClinVar RCV Id: RCV000708658 RCV000792860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln2615Glu
CA6266202
NM_001351834.2:c.7843C>G