Canonical Allele Identifier: PA2827956090
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 572572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn637Ser
CA16025430
NM_001354897.2:c.1910A>G