Canonical Allele Identifier: PA100802
Gene: ERBB4 HGNC NCBI

Linked Data

ClinVar Variation Id: 64626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005226.1:p.Arg1275Trp
CA216502
NM_005235.3:c.3823C>T