Canonical Allele Identifier: PA2826262035
Gene: CRHR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2610342
ClinVar RCV Id: RCV004355727

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189410.1:p.Asn330Asp
CA156078599
NM_001202481.1:c.988A>G