Canonical Allele Identifier: PA1139739400
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 955939
ClinVar RCV Id: RCV001228660 RCV003325552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly2020Val
CA382550034
NM_001351834.2:c.6059G>T