Canonical Allele Identifier: PA2825034472
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 826169

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys2025Asn
CA382550116
NM_000051.4:c.6075G>T
CA382550118
NM_000051.4:c.6075G>C