Canonical Allele Identifier: PA2825016454
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2746817
ClinVar RCV Id: RCV003536583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Tyr737Phe
CA16026174
NM_000038.6:c.2210A>T