Canonical Allele Identifier: PA2826262061
Gene: CRHR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2610342
ClinVar RCV Id: RCV004355727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189411.1:p.Asn343Asp
CA156078599
NM_001202482.2:c.1027A>G