Canonical Allele Identifier: PA2825031253
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1779005
ClinVar RCV Id: RCV002399197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met577Ile
CA382535303
NM_000051.4:c.1731G>C
CA382535304
NM_000051.4:c.1731G>T
CA382535305
NM_000051.4:c.1731G>A