Canonical Allele Identifier: PA2827961691
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418637
ClinVar RCV Id: RCV000485956 RCV000582404 RCV003651918 RCV004002263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn2350His
CA046653
NM_001354897.2:c.7048A>C