Canonical Allele Identifier: PA196934
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 187178
ClinVar RCV Id: RCV000166878 RCV000474811 RCV000478109 RCV002498828 RCV003315416
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp831Gly
CA196932
NM_000051.4:c.2492A>G