Canonical Allele Identifier: PA2580205101
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2447496
ClinVar RCV Id: RCV003176473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Tyr2019Phe
CA382550017
NM_001351834.2:c.6056A>T