Canonical Allele Identifier: PA275898
Gene: GRHPR HGNC NCBI

Linked Data

ClinVar Variation Id: 204238
ClinVar RCV Id: RCV000186445

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036335.1:p.Asn312Asp
CA275897
NM_012203.2:c.934A>G