Canonical Allele Identifier: PA273237
Gene: STRC HGNC NCBI

Linked Data

ClinVar Variation Id: 165311
ClinVar RCV Id: RCV000151950 RCV000225023 RCV000494575 RCV002467597 RCV003398799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714544.1:p.Arg1391Gly
CA273236
NM_153700.2:c.4171C>G