Canonical Allele Identifier: PA2827629499
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3232057
ClinVar RCV Id: RCV004518772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Met437Ile
CA382533636
NM_001351834.2:c.1311G>A
CA382533637
NM_001351834.2:c.1311G>T
CA382533639
NM_001351834.2:c.1311G>C