Canonical Allele Identifier: PA2827962600
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 652208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn2628Ser
CA16038396
NM_001354897.2:c.7883A>G