Canonical Allele Identifier: PA916033905
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 233776
ClinVar RCV Id: RCV000221486 RCV000533728 RCV001174836 RCV003227722
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr2113Ser
CA6265906
NM_001351834.2:c.6338C>G
CA382552309
NM_001351834.2:c.6337A>T