Canonical Allele Identifier: PA658820194
Gene: HECW2 HGNC NCBI

Linked Data

ClinVar Variation Id: 523073
ClinVar RCV Id: RCV000626283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065811.1:p.Thr914Met
CA2037982
NM_020760.4:c.2741C>T