Canonical Allele Identifier: PA2825031155
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1403123
ClinVar RCV Id: RCV001925276

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Pro537Arg
CA382534473
NM_000051.4:c.1610C>G