Canonical Allele Identifier: PA2825802459
Gene: SPATA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2303716
ClinVar RCV Id: RCV004148812

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129245.1:p.Pro491Ala
CA408945439
NM_001135773.2:c.1471C>G