Canonical Allele Identifier: PA2825035179
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 860092
ClinVar RCV Id: RCV001066337
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser2329Thr
CA382557786
NM_000051.4:c.6986G>C