Allele Registry

Canonical Allele Identifier: PA110568

Gene: POU1F1 HGNC NCBI

ClinVar Allele:

28648

ClinVar RCV:

RCV000014579

ClinVar Variation:

13609

HGVS (amino-acid)	Matching Registered Transcripts
NP_000297.1:p.Pro239Ser	CA250616 NM_000306.4:c.715C>T