Canonical Allele Identifier: PA2827954288
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1016218
ClinVar RCV Id: RCV003652157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr27Ser
CA360611894
NM_001354897.2:c.79A>T
CA360611900
NM_001354897.2:c.80C>G