Allele Registry

Canonical Allele Identifier: PA2827992297

Gene: APC HGNC NCBI

ClinVar Allele:

49958

ClinVar RCV:

RCV000034404

RCV000035065

RCV000144567

RCV000159535

RCV003904891

RCV004018732

ClinVar Variation:

41519

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341830.1:p.Ser476Phe	CA005357 NM_001354901.2:c.1427C>T