Canonical Allele Identifier: PA2825031863
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 848252

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met855Val
CA382543805
NM_000051.4:c.2563A>G