Canonical Allele Identifier: PA2827968516
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro1609Leu
CA040139
NM_001354898.2:c.4826C>T