Canonical Allele Identifier: PA891866311
Gene: HECW2 HGNC NCBI

Linked Data

ClinVar Variation Id: 391956
ClinVar RCV Id: RCV000425494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335697.1:p.Arg861Trp
CA16604090
NM_001348768.2:c.2581C>T