Canonical Allele Identifier: PA2825034075
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2679706
ClinVar RCV Id: RCV003466614

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu1842Pro
CA382545833
NM_000051.4:c.5525T>C