Canonical Allele Identifier: PA110601
Gene: CSRP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 8777
ClinVar RCV Id: RCV000009322 RCV002399315
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003467.1:p.Cys58Gly
CA119911
NM_003476.4:c.172T>G