Canonical Allele Identifier: PA275886
Gene: GRHPR HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036335.1:p.Leu68Pro
CA275885
NM_012203.2:c.203T>C