Canonical Allele Identifier: PA658670574
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453708
ClinVar RCV Id: RCV000548687 RCV004023656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu2630Val
CA382561448
NM_000051.4:c.7888T>G