Canonical Allele Identifier: PA913191719
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 630763
ClinVar RCV Id: RCV000776758 RCV001298948
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Pro2056Leu
CA382550667
NM_000051.4:c.6167C>T