Canonical Allele Identifier: PA2827964519
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2755578
ClinVar RCV Id: RCV003536840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp372Glu
CA16023913
NM_001354898.2:c.1116C>A
CA16023914
NM_001354898.2:c.1116C>G