Canonical Allele Identifier: PA177648
Gene: POU3F4 HGNC NCBI

Linked Data

ClinVar Variation Id: 164973
ClinVar RCV Id: RCV000151667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000298.3:p.Ser161Arg
CA177647
NM_000307.5:c.483C>A
CA413751618
NM_000307.5:c.481A>C
CA413751624
NM_000307.5:c.483C>G