Canonical Allele Identifier: PA2827962570
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3074632
ClinVar RCV Id: RCV004014166
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala2618Val
CA16038328
NM_001354897.2:c.7853C>T