Canonical Allele Identifier: PA645468547
Gene: STRC HGNC NCBI

Linked Data

ClinVar Variation Id: 227969
ClinVar RCV Id: RCV000221308 RCV001796729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714544.1:p.Val1467Ile
CA7528037
NM_153700.2:c.4399G>A