Canonical Allele Identifier: PA658812237
Gene: STRC HGNC NCBI

Linked Data

ClinVar Variation Id: 505743
ClinVar RCV Id: RCV000604778
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714544.1:p.Ser1710Lys
CA658798322
NM_153700.2:c.5129_5130delinsAG