Canonical Allele Identifier: PA298095
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181903
ClinVar RCV Id: RCV000159666 RCV000543356 RCV001021590 RCV001193630
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn133Ile
CA298093
NM_000051.4:c.398A>T