Canonical Allele Identifier: PA916041991
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489434
ClinVar RCV Id: RCV000580480
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp993His
CA16028016
NM_001354898.2:c.2977G>C