Canonical Allele Identifier: PA2827989872
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 647268

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2539Phe
CA16038139
NM_001354900.2:c.7616C>T