Canonical Allele Identifier: PA645485387
Gene: SPEF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 403474
ClinVar RCV Id: RCV000455441 RCV001692122
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079143.3:p.Asp500Asn
CA3230495
NM_024867.4:c.1498G>A