Canonical Allele Identifier: PA108618
Gene: TRPV4 HGNC NCBI

Linked Data

ClinVar Variation Id: 4998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067638.3:p.Pro799Leu
CA117176
NM_021625.5:c.2396C>T