Canonical Allele Identifier: PA2580129046
Gene: SPANXN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2212505
ClinVar RCV Id: RCV004082056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001009615.1:p.Thr61Met
CA10534795
NM_001009615.3:c.182C>T