Canonical Allele Identifier: PA2825031429
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 935510
ClinVar RCV Id: RCV001204120

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln654His
CA382536784
NM_000051.4:c.1962G>C
CA382536785
NM_000051.4:c.1962G>T