Canonical Allele Identifier: PA2825025770
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro2831Leu
CA050906
NM_000038.6:c.8492C>T