Canonical Allele Identifier: PA916034763
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 220614
ClinVar RCV Id: RCV000204614 RCV000218858 RCV003468957 RCV003483574 RCV004526643 RCV000484197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala2798Asp
CA348832
NM_001351834.2:c.8393C>A