Canonical Allele Identifier: PA206575
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Pro1354Thr
CA206573
NM_000051.4:c.4060C>A