Canonical Allele Identifier: PA16040165
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gln2804His
CA10582345
NM_000038.6:c.8412G>T
CA16039584
NM_000038.6:c.8412G>C