Canonical Allele Identifier: PA2827962582
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537451
ClinVar RCV Id: RCV003538442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Trp2622Cys
CA16038354
NM_001354897.2:c.7866G>C
CA16038355
NM_001354897.2:c.7866G>T