Canonical Allele Identifier: PA2825031922
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2698356
ClinVar RCV Id: RCV003501027
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln876Glu
CA382544288
NM_000051.4:c.2626C>G