Canonical Allele Identifier: PA2825030621
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2087496
ClinVar RCV Id: RCV003017866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu304Asp
CA382530487
NM_000051.4:c.912A>C
CA382530488
NM_000051.4:c.912A>T