Canonical Allele Identifier: PA916041594
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 652208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn2636Ser
CA16038396
NM_001354896.2:c.7907A>G