Canonical Allele Identifier: PA211349
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 161206
ClinVar RCV Id: RCV000148363 RCV000159544 RCV000168133 RCV000567920 RCV001704072 RCV003534394 RCV003917461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Met949Ile
CA007863
NM_001127510.3:c.2847G>T
CA16027540
NM_001127510.3:c.2847G>A
CA16027541
NM_001127510.3:c.2847G>C