Canonical Allele Identifier: PA2827954387
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1372129
ClinVar RCV Id: RCV003772626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Trp54Ser
CA360612212
NM_001354897.2:c.161G>C