Canonical Allele Identifier: PA2827983532
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411407

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser602Phe
CA16025529
NM_001354900.2:c.1805C>T