Canonical Allele Identifier: PA2825034565
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2700587
ClinVar RCV Id: RCV003501083
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile2064Met
CA382550781
NM_000051.4:c.6192C>G