Canonical Allele Identifier: PA211348
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 161206
ClinVar RCV Id: RCV000148363 RCV000159544 RCV000168133 RCV000567920 RCV001704072 RCV003534394 RCV003917461
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Met949Ile
CA007863
NM_000038.6:c.2847G>T
CA16027540
NM_000038.6:c.2847G>A
CA16027541
NM_000038.6:c.2847G>C