Canonical Allele Identifier: PA234983
Gene: SPATA7 HGNC NCBI

Linked Data

ClinVar Variation Id: 167716
ClinVar RCV Id: RCV000153988 RCV001049973 RCV001120978 RCV003888597
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060888.2:p.Met345Val
CA234982
NM_018418.5:c.1033A>G