Canonical Allele Identifier: PA916031703
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 219386
ClinVar RCV Id: RCV000206511
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Pro424Leu
CA350530
NM_001351834.2:c.1271C>T