Canonical Allele Identifier: PA2825035832
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 827300
ClinVar RCV Id: RCV001026895
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp2625His
CA382561418
NM_000051.4:c.7873G>C