Canonical Allele Identifier: PA658812234
Gene: STRC HGNC NCBI

Linked Data

ClinVar Variation Id: 504929
ClinVar RCV Id: RCV000614036
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714544.1:p.Val1635Ala
CA392160626
NM_153700.2:c.4904T>C