Canonical Allele Identifier: PA2580138266
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 2127368
ClinVar RCV Id: RCV003055464

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077354.2:p.Met78Val
CA198634597
NM_001083885.3:c.232A>G