Canonical Allele Identifier: PA180703
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 177752
ClinVar RCV Id: RCV000154365 RCV000964640
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.His364Arg
CA180702
NM_015404.4:c.1091A>G