Canonical Allele Identifier: PA2580167986
Gene: RSPH4A HGNC NCBI

Linked Data

ClinVar Variation Id: 2414164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155136.1:p.Val315Ile
CA365402993
NM_001161664.2:c.943G>A