Canonical Allele Identifier: PA916033023
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 188194
ClinVar RCV Id: RCV000168111 RCV000220668 RCV000478130 RCV000780906 RCV003468825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys1435Thr
CA334280
NM_001351834.2:c.4304A>C