Canonical Allele Identifier: PA2828009271
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro1543Leu
CA040139
NM_001354902.2:c.4628C>T