Canonical Allele Identifier: PA2825035684
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1055422
ClinVar RCV Id: RCV001364089 RCV001773723 RCV004550086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu2557Trp
CA382560971
NM_000051.4:c.7670T>G