Canonical Allele Identifier: PA2828049071
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 565362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro2539Ser
CA16038695
NM_001354904.2:c.7615C>T