Canonical Allele Identifier: PA286992
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127446
ClinVar RCV Id: RCV000115252 RCV000195623 RCV000488003 RCV000780920 RCV000786770 RCV003325459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu2492Arg
CA286990
NM_000051.4:c.7475T>G