Canonical Allele Identifier: PA891845379
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 574618

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Cys2624Ser
CA6266205
NM_000051.4:c.7871G>C
CA382561411
NM_000051.4:c.7870T>A