Canonical Allele Identifier: PA2827982947
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2822243
ClinVar RCV Id: RCV003650976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Cys388Ser
CA16024236
NM_001354900.2:c.1162T>A
CA16024240
NM_001354900.2:c.1163G>C