Canonical Allele Identifier: PA260039
Gene: C19orf12 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242976.1:p.Leu121Gln
CA260038
NM_001256047.2:c.362T>A