Canonical Allele Identifier: PA136897
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 45662
ClinVar RCV Id: RCV000038880 RCV001213992
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Val566Leu
CA136896
NM_015404.4:c.1696G>C
CA374621112
NM_015404.4:c.1696G>T