Canonical Allele Identifier: PA2573204636
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1473185
ClinVar RCV Id: RCV001977428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Met838Ile
CA382543412
NM_001351834.2:c.2514G>A
CA382543414
NM_001351834.2:c.2514G>C
CA382543416
NM_001351834.2:c.2514G>T