Canonical Allele Identifier: PA2825363329
Gene: SPATA7 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035518.1:p.Asn31Asp
CA390545441
NM_001040428.4:c.91A>G