Canonical Allele Identifier: PA338757
Gene: TRPV4 HGNC NCBI

Linked Data

ClinVar Variation Id: 215918
ClinVar RCV Id: RCV000199632 RCV000278046 RCV000293468 RCV000328738 RCV000332180 RCV000389025 RCV000592513 RCV001701706 RCV001174133 RCV002399742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067638.3:p.Ile516Val
CA338755
NM_021625.5:c.1546A>G