Canonical Allele Identifier: PA2827960690
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485114
ClinVar RCV Id: RCV000563143 RCV003652034 RCV004001101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp2046Asn
CA16034696
NM_001354897.2:c.6136G>A