Canonical Allele Identifier: PA645498368
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407737
ClinVar RCV Id: RCV000467719 RCV002255389
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu186Phe
CA16613247
NM_000051.4:c.558A>C
CA382527759
NM_000051.4:c.558A>T