Canonical Allele Identifier: PA645498352
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407585
ClinVar RCV Id: RCV000467265 RCV000579672
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu176Val
CA6264627
NM_000051.4:c.526C>G