Canonical Allele Identifier: PA2580474623
Gene: RSPH6A HGNC NCBI

Linked Data

ClinVar Variation Id: 2246773
ClinVar RCV Id: RCV004106444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110412.1:p.Glu505Val
CA406404856
NM_030785.4:c.1514A>T