Canonical Allele Identifier: PA2825031177
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1331886
ClinVar RCV Id: RCV001804402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu546Met
CA382534523
NM_000051.4:c.1636C>A