Canonical Allele Identifier: PA658670623
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Pro2665Ala
CA382561783
NM_000051.4:c.7993C>G