Canonical Allele Identifier: PA2580415127
Gene: SPA17 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_059121.1:p.Asn54Ser
CA230369966
NM_017425.4:c.161A>G