Canonical Allele Identifier: PA658673477
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481336
ClinVar RCV Id: RCV000561372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys215Thr
CA382528496
NM_000051.4:c.644A>C