Canonical Allele Identifier: PA2825353579
Gene: C19orf12 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026896.3:p.Leu121Gln
CA260038
NM_001031726.4:c.362T>A