Canonical Allele Identifier: PA2825024898
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2861029
ClinVar RCV Id: RCV003743178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Trp2612Ser
CA16038351
NM_000038.6:c.7835G>C