Canonical Allele Identifier: PA2827971700
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gln2580His
CA16038310
NM_001354898.2:c.7740A>C
CA16038311
NM_001354898.2:c.7740A>T