Canonical Allele Identifier: PA645498943
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val320Met
CA16613057
NM_000051.4:c.958G>A