Canonical Allele Identifier: PA108489
Gene: TRPV4 HGNC NCBI

Linked Data

ClinVar Variation Id: 4997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067638.3:p.Ile331Phe
CA117174
NM_021625.5:c.991A>T