Canonical Allele Identifier: PA2828012542
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 939073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2536Phe
CA049365
NM_001354902.2:c.7607C>T