Canonical Allele Identifier: PA2825030115
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1038712
ClinVar RCV Id: RCV001342054

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile77Leu
CA382521452
NM_000051.4:c.229A>C
CA382521456
NM_000051.4:c.229A>T