Canonical Allele Identifier: PA658812227
Gene: STRC HGNC NCBI

Linked Data

ClinVar Variation Id: 504678
ClinVar RCV Id: RCV000601781 RCV004024886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714544.1:p.Thr1478Pro
CA7528034
NM_153700.2:c.4432A>C