Canonical Allele Identifier: PA658674176
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482587
ClinVar RCV Id: RCV000568067 RCV000627991 RCV003226325 RCV003465222
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys940Ile
CA6265116
NM_000051.4:c.2819A>T