Canonical Allele Identifier: PA2827336159
Gene: WASHC5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1162
ClinVar Variation Id: 39008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317538.1:p.Leu471Phe
CA251713
NM_001330609.2:c.1413G>C
CA343118
NM_001330609.2:c.1413G>T