Canonical Allele Identifier: PA298166
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181928
ClinVar RCV Id: RCV000159693 RCV000254631 RCV000472551 RCV001704147 RCV001355809 RCV003149969
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala799Val
CA298164
NM_000051.4:c.2396C>T