Canonical Allele Identifier: PA166135
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141688
ClinVar RCV Id: RCV000130302 RCV000198440 RCV000236652 RCV001154640 RCV003315888 RCV003743588 RCV003479014 RCV003492599 RCV003998054
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Glu1209Lys
CA008564
NM_001127510.3:c.3625G>A