Canonical Allele Identifier: PA354961
Gene: RPH3A HGNC NCBI

Linked Data

ClinVar Variation Id: 224156
ClinVar RCV Id: RCV000209913
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137326.1:p.Thr450Ser
CA354959
NM_001143854.2:c.1349C>G
CA386786492
NM_001143854.2:c.1348A>T