Canonical Allele Identifier: PA279623
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 217857
ClinVar RCV Id: RCV000201908
ClinVar Variation Id: 375885
ClinVar RCV Id: RCV000434421
ClinVar Variation Id: 376712
ClinVar RCV Id: RCV000432633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004295.2:p.Phe1245Leu
CA279621
NM_004304.5:c.3735C>A
CA16602368
NM_004304.5:c.3735C>G
CA16603122
NM_004304.5:c.3733T>C