Canonical Allele Identifier: PA2827959430
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1051201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn1660Ser
CA040262
NM_001354897.2:c.4979A>G