Canonical Allele Identifier: PA2825014628
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2844378
ClinVar RCV Id: RCV003652473

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser384Arg
CA16023822
NM_000038.6:c.1150A>C
CA16023828
NM_000038.6:c.1152T>A
CA16023829
NM_000038.6:c.1152T>G