Canonical Allele Identifier: PA645500529
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407501
ClinVar Variation Id: 937882
ClinVar RCV Id: RCV001207000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys659Asn
CA16613349
NM_000051.4:c.1977G>T
CA382536859
NM_000051.4:c.1977G>C