Canonical Allele Identifier: PA645504161
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 231842
ClinVar RCV Id: RCV000222696 RCV002221518
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr2640Ser
CA10579274
NM_000051.4:c.7919C>G
CA382561513
NM_000051.4:c.7918A>T