Allele Registry

Canonical Allele Identifier: PA2826952904

Gene: PCNT HGNC NCBI

ClinVar RCV:

RCV000147250

RCV000603118

RCV001711590

ClinVar Variation:

159697

HGVS (amino-acid)	Matching Registered Transcripts
NP_001302458.1:p.Arg3048Ser	CA173148 NM_001315529.2:c.9144A>C CA410579389 NM_001315529.2:c.9144A>T