Canonical Allele Identifier: PA658660778
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470103
ClinVar RCV Id: RCV000532913 RCV001026682 RCV003742793 RCV003999431 RCV002231508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2556Leu
CA048890
NM_001127510.3:c.7667C>T