Canonical Allele Identifier: PA108589
Gene: TRPV4 HGNC NCBI

Linked Data

ClinVar Variation Id: 126472
ClinVar RCV Id: RCV000202452 RCV001596963 RCV003505098
ClinVar Variation Id: 1453327
ClinVar RCV Id: RCV002002352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067638.3:p.Phe617Leu
CA347704
NM_021625.5:c.1851C>A
CA386651798
NM_021625.5:c.1851C>G
CA386651803
NM_021625.5:c.1849T>C