Canonical Allele Identifier: PA2827962523
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2841190
ClinVar RCV Id: RCV003652389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Val2602Leu
CA16038220
NM_001354897.2:c.7804G>C
CA16038221
NM_001354897.2:c.7804G>T