Canonical Allele Identifier: PA2825031255
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 819965
ClinVar RCV Id: RCV001012942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys578Asn
CA382535312
NM_000051.4:c.1734A>C
CA382535313
NM_000051.4:c.1734A>T