Canonical Allele Identifier: PA2825031854
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3232502
ClinVar RCV Id: RCV004521178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu850Asp
CA382543708
NM_000051.4:c.2550G>C
CA382543710
NM_000051.4:c.2550G>T