Canonical Allele Identifier: PA913200310
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 631456
ClinVar RCV Id: RCV000777890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Val1776Leu
CA16032974
NM_001127510.3:c.5326G>C
CA16032975
NM_001127510.3:c.5326G>T