Canonical Allele Identifier: PA658801442
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 524229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser1250Tyr
CA382524188
NM_000051.4:c.3749C>A