Canonical Allele Identifier: PA127327
Gene: BDNF HGNC NCBI

Linked Data

ClinVar Variation Id: 17697

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733931.1:p.Val66Met
CA127325
NM_170735.6:c.196G>A