Canonical Allele Identifier: PA2825033201
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 847462
ClinVar RCV Id: RCV001051010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val1446Ile
CA382531931
NM_000051.4:c.4336G>A