Canonical Allele Identifier: PA891845252
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 572732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn1855Lys
CA382546051
NM_000051.4:c.5565T>A
CA382546053
NM_000051.4:c.5565T>G