Canonical Allele Identifier: PA645500535
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile665Val
CA16613020
NM_000051.4:c.1993A>G