Canonical Allele Identifier: PA645504031
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 236777
ClinVar RCV Id: RCV000232658 RCV000564111
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met2550Val
CA10582855
NM_000051.4:c.7648A>G