Canonical Allele Identifier: PA2825031386
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1171142
ClinVar RCV Id: RCV001524063

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.His636Pro
CA382536305
NM_000051.4:c.1907A>C