Canonical Allele Identifier: PA658670613
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453712
ClinVar RCV Id: RCV000775848 RCV000555928 RCV003464124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu2660Asp
CA382561757
NM_000051.4:c.7980A>C
CA382561758
NM_000051.4:c.7980A>T