Canonical Allele Identifier: PA2825033152
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2846494
ClinVar RCV Id: RCV003605213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala1427Ser
CA382531343
NM_000051.4:c.4279G>T