Canonical Allele Identifier: PA658674134
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482686
ClinVar RCV Id: RCV000567976 RCV000628030
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn883Lys
CA382545014
NM_000051.4:c.2649T>A
CA382545015
NM_000051.4:c.2649T>G