Canonical Allele Identifier: PA658660054
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro1634Leu
CA040139
NM_001127510.3:c.4901C>T