Canonical Allele Identifier: PA916034340
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 231789
ClinVar RCV Id: RCV000220077 RCV002247654 RCV000528764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Tyr2470Asp
CA10579258
NM_001351834.2:c.7408T>G