Canonical Allele Identifier: PA2828003968
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1320471
ClinVar RCV Id: RCV001776450
ClinVar Variation Id: 2573820
ClinVar RCV Id: RCV003318156
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gln2312His
CA16037029
NM_001354902.2:c.6936G>C
CA16037030
NM_001354902.2:c.6936G>T