Canonical Allele Identifier: PA2827959612
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 825464

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser1717Phe
CA16032523
NM_001354897.2:c.5150C>T