Canonical Allele Identifier: PA2828012267
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2464Leu
CA16037984
NM_001354902.2:c.7391C>T