Canonical Allele Identifier: PA1139752029
Gene: KCNV2 HGNC NCBI

Linked Data

ClinVar Variation Id: 834167

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598004.1:p.Pro537Ser
CA4965952
NM_133497.4:c.1609C>T