Allele Registry

Canonical Allele Identifier: PA108589

Gene: TRPV4 HGNC NCBI

ClinVar RCV:

RCV000202452

RCV001596963

RCV002002352

RCV003505098

ClinVar Variation:

126472

1453327

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