Allele Registry

Canonical Allele Identifier: PA173149

Gene: PCNT HGNC NCBI

ClinVar RCV:

RCV000147250

RCV000603118

RCV001711590

ClinVar Variation:

159697

HGVS (amino-acid)	Matching Registered Transcripts
NP_006022.3:p.Arg3245Ser	CA173148 NM_006031.5:c.9735A>C CA410579389 NM_006031.5:c.9735A>T