Canonical Allele Identifier: PA156664
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 133482
ClinVar RCV Id: RCV000119986 RCV000460983 RCV002256051 RCV003223611
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004295.2:p.Pro367Arg
CA156662
NM_004304.5:c.1100C>G