Canonical Allele Identifier: PA658661011
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro2831Leu
CA050906
NM_001127510.3:c.8492C>T