Canonical Allele Identifier: PA2827976621
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127291
ClinVar RCV Id: RCV000115088 RCV000562223 RCV003764811
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gly1284Ala
CA008783
NM_001354899.2:c.3851G>C