Canonical Allele Identifier: PA2827970676
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 644645

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2270Ala
CA16036352
NM_001354898.2:c.6808T>G