Canonical Allele Identifier: PA2742023965
Gene: GCC2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852118.2:p.Glu506Lys
CA1820544
NM_181453.4:c.1516G>A