Canonical Allele Identifier: PA2828014547
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2105910
ClinVar RCV Id: RCV003744912 RCV003585333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr27Ser
CA16023339
NM_001354906.2:c.79A>T
CA16023341
NM_001354906.2:c.80C>G