Canonical Allele Identifier: PA658743639
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 490650
ClinVar RCV Id: RCV000582226 RCV000628057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.His2125Leu
CA382553260
NM_000051.4:c.6374A>T