Canonical Allele Identifier: PA658660915
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro2712Ala
CA049967
NM_001127510.3:c.8134C>G