Canonical Allele Identifier: PA198115
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 187621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile2844Val
CA198113
NM_000051.4:c.8530A>G