Canonical Allele Identifier: PA2829354977
Gene: CRHR2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001874.2:p.Asn344Asp
CA156078599
NM_001883.5:c.1030A>G