Canonical Allele Identifier: PA156652
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 133478
ClinVar RCV Id: RCV000119982 RCV000731883 RCV001087719 RCV002257416
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004295.2:p.Ala1396Thr
CA156650
NM_004304.5:c.4186G>A