Canonical Allele Identifier: PA2827954371
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 548731
ClinVar RCV Id: RCV000662474
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Trp50Ser
CA360612166
NM_001354897.2:c.149G>C