Canonical Allele Identifier: PA2825036001
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2811082
ClinVar RCV Id: RCV003606174

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile2701Leu
CA6266273
NM_000051.4:c.8101A>T
CA382562103
NM_000051.4:c.8101A>C