Canonical Allele Identifier: PA658671308
Gene: STRC HGNC NCBI

Linked Data

ClinVar Variation Id: 450926
ClinVar RCV Id: RCV000523652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714544.1:p.Asp1561His
CA7527950
NM_153700.2:c.4681G>C