Canonical Allele Identifier: PA2825030673
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 823469
ClinVar RCV Id: RCV001019732 RCV001860957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile326Leu
CA382531101
NM_000051.4:c.976A>C
CA382531105
NM_000051.4:c.976A>T