Canonical Allele Identifier: PA658812245
Gene: STRC HGNC NCBI

Linked Data

ClinVar Variation Id: 505196
ClinVar RCV Id: RCV000610766 RCV000993097 RCV002467921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714544.1:p.Trp1734Arg
CA7527782
NM_153700.2:c.5200T>C
CA392158152
NM_153700.2:c.5200T>A