Allele Registry

Canonical Allele Identifier: PA16039864

Gene: APC HGNC NCBI

ClinVar Variation Id: 231954

HGVS (amino-acid)	Matching Registered Transcripts
NP_000029.2:p.Ser634Arg	CA10578330 NM_000038.6:c.1902T>G CA16025473 NM_000038.6:c.1900A>C CA16025479 NM_000038.6:c.1902T>A