Canonical Allele Identifier: PA210918
Gene: STRC HGNC NCBI

Linked Data

ClinVar Variation Id: 156030
ClinVar RCV Id: RCV000144091 RCV000151965 RCV001682842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714544.1:p.Phe60Ser
CA210917
NM_153700.2:c.179T>C