Canonical Allele Identifier: PA2825014097
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 822781
ClinVar RCV Id: RCV001018420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser295Arg
CA16023248
NM_000038.6:c.883A>C
CA16023252
NM_000038.6:c.885T>A
CA16023253
NM_000038.6:c.885T>G