Canonical Allele Identifier: PA2825032002
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2128891
ClinVar RCV Id: RCV003040265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln912His
CA382545373
NM_000051.4:c.2736G>T
CA382545375
NM_000051.4:c.2736G>C