Canonical Allele Identifier: PA658812877
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 504565
ClinVar RCV Id: RCV000611623 RCV001049406 RCV001165877 RCV001165878
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Met461Leu
CA5205980
NM_015404.4:c.1381A>C
CA374608498
NM_015404.4:c.1381A>T