Canonical Allele Identifier: PA2825024358
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2815299
ClinVar RCV Id: RCV003744126

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Arg2470Ser
CA16037460
NM_000038.6:c.7410A>C
CA16037461
NM_000038.6:c.7410A>T