Canonical Allele Identifier: PA645504109
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407490
ClinVar RCV Id: RCV000485307 RCV000474353 RCV000565171
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile2606Met
CA16613132
NM_000051.4:c.7818A>G