Canonical Allele Identifier: PA2827970888
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 958591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2334Ala
CA046787
NM_001354898.2:c.7000T>G