Canonical Allele Identifier: PA2825032980
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2874074
ClinVar RCV Id: RCV003605573
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu1340Phe
CA382527627
NM_000051.4:c.4020A>C
CA382527634
NM_000051.4:c.4020A>T