Canonical Allele Identifier: PA2827965143
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 919879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn577Ser
CA16025270
NM_001354898.2:c.1730A>G