Canonical Allele Identifier: PA108626
Gene: TRPV4 HGNC NCBI

Linked Data

ClinVar Variation Id: 18431

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067638.3:p.Pro799Ser
CA117189
NM_021625.5:c.2395C>T