Canonical Allele Identifier: PA2827630059
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2835245
ClinVar RCV Id: RCV003606528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338764.1:p.Gln51del
CA198174
NM_001351835.2:c.151C>T
CA2739270897
NM_001351835.2:c.151_153del