Canonical Allele Identifier: PA2825031853
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 821467

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val849Leu
CA382543674
NM_000051.4:c.2545G>C
CA382543676
NM_000051.4:c.2545G>T