Canonical Allele Identifier: PA658812235
Gene: STRC HGNC NCBI

Linked Data

ClinVar Variation Id: 505381
ClinVar RCV Id: RCV000607453 RCV003403414 RCV003480710
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714544.1:p.Thr1709Ala
CA392158589
NM_153700.2:c.5125A>G