Canonical Allele Identifier: PA2825024899
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537451
ClinVar RCV Id: RCV003538442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Trp2612Cys
CA16038354
NM_000038.6:c.7836G>C
CA16038355
NM_000038.6:c.7836G>T