Canonical Allele Identifier: PA2825031802
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2834021
ClinVar RCV Id: RCV003606503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys828Asn
CA382543219
NM_000051.4:c.2484G>C
CA382543220
NM_000051.4:c.2484G>T