Canonical Allele Identifier: PA645501303
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407726
ClinVar RCV Id: RCV000467358 RCV001524356
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu937Asp
CA16613310
NM_000051.4:c.2811A>C
CA382545725
NM_000051.4:c.2811A>T