Canonical Allele Identifier: PA2825036101
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 948181
ClinVar RCV Id: RCV001219390
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met2734Ile
CA382562563
NM_000051.4:c.8202G>A
CA382562564
NM_000051.4:c.8202G>C
CA382562565
NM_000051.4:c.8202G>T