Canonical Allele Identifier: PA16039850
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 246087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Lys516Asn
CA10584241
NM_000038.6:c.1548G>C
CA16024690
NM_000038.6:c.1548G>T