Canonical Allele Identifier: PA645504177
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 234142
ClinVar RCV Id: RCV000218059 RCV001048572
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala2649Val
CA10579277
NM_000051.4:c.7946C>T