Canonical Allele Identifier: PA341965
Gene: TFAP2B HGNC NCBI

Linked Data

ClinVar Variation Id: 21358
ClinVar RCV Id: RCV000020530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003212.2:p.Asp148Glu
CA341964
NM_003221.4:c.444C>A
CA364412960
NM_003221.4:c.444C>G