Allele Registry

Canonical Allele Identifier: PA2826117925

Gene: TRPV4 HGNC NCBI

ClinVar RCV:

RCV000202527

ClinVar Variation:

126468

HGVS (amino-acid)	Matching Registered Transcripts
NP_001170904.1:p.Phe485Leu	CA347771 NM_001177433.1:c.1453T>C CA386652212 NM_001177433.1:c.1455C>G CA386652213 NM_001177433.1:c.1455C>A