Canonical Allele Identifier: PA16039886
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236574

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Leu831Ser
CA10582297
NM_000038.6:c.2492T>C