Canonical Allele Identifier: PA2825184073
Gene: MC2R HGNC NCBI

Linked Data

ClinVar Variation Id: 1206335
ClinVar RCV Id: RCV001573869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000520.1:p.Trp297Arg
CA401993492
NM_000529.2:c.889T>C
CA401993494
NM_000529.2:c.889T>A