Canonical Allele Identifier: PA916041964
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Leu466Phe
CA10578315
NM_001354897.2:c.1396C>T