Canonical Allele Identifier: PA176052
Gene: ESPN HGNC NCBI

Linked Data

ClinVar Variation Id: 163412
ClinVar RCV Id: RCV000150656 RCV000477776 RCV000885850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_113663.2:p.Pro350Ser
CA176051
NM_031475.3:c.1048C>T