Canonical Allele Identifier: PA916014070
Gene: C19orf12 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269860.1:p.Leu57Gln
CA260038
NM_001282931.3:c.170T>A