Canonical Allele Identifier: PA916041888
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135682
ClinVar RCV Id: RCV000122755 RCV002345429 RCV003997368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Arg411Ser
CA004084
NM_001354897.2:c.1233G>T
CA16023939
NM_001354897.2:c.1233G>C