Canonical Allele Identifier: PA2829758086
Gene: FAF2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055428.1:p.Tyr230Cys
CA362257033
NM_014613.3:c.689A>G