Canonical Allele Identifier: PA2826262017
Gene: CRHR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2597682
ClinVar RCV Id: RCV004342974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189410.1:p.Ile101Val
CA4206599
NM_001202481.1:c.301A>G