Canonical Allele Identifier: PA916031568
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407663
ClinVar RCV Id: RCV000466092
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Tyr332Phe
CA16613307
NM_001351834.2:c.995A>T