Canonical Allele Identifier: PA2825035126
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3222656
ClinVar RCV Id: RCV004516040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln2305His
CA382557051
NM_000051.4:c.6915G>C
CA382557052
NM_000051.4:c.6915G>T