Canonical Allele Identifier: PA2827959375
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro1644Leu
CA040139
NM_001354897.2:c.4931C>T