Canonical Allele Identifier: PA2827950837
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236585
ClinVar RCV Id: RCV000486957 RCV000708638 RCV003535606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gln1053His
CA10582304
NM_001354896.2:c.3159G>T
CA16028136
NM_001354896.2:c.3159G>C