Canonical Allele Identifier: PA2825036020
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1021521
ClinVar RCV Id: RCV001321301 RCV003120549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp2708Val
CA382562168
NM_000051.4:c.8123A>T