Canonical Allele Identifier: PA2825033038
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2754315
ClinVar RCV Id: RCV003500086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp1367Glu
CA382528602
NM_000051.4:c.4101C>A
CA382528604
NM_000051.4:c.4101C>G