Canonical Allele Identifier: PA2827961779
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 659672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro2379Leu
CA16036808
NM_001354897.2:c.7136C>T