Canonical Allele Identifier: PA2825034953
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2007318
ClinVar RCV Id: RCV002842228

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met2235Ile
CA382554961
NM_000051.4:c.6705G>A
CA382554964
NM_000051.4:c.6705G>C
CA382554966
NM_000051.4:c.6705G>T