Canonical Allele Identifier: PA916032917
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 216210
ClinVar RCV Id: RCV000196770 RCV003165465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asn1339Lys
CA336702
NM_001351834.2:c.4017T>G
CA382527609
NM_001351834.2:c.4017T>A