ClinGen Allele Registry
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Canonical Allele Identifier:
PA123862
Gene: MC1R
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000015377
RCV000347221
RCV000662303
RCV000851264
RCV001080639
RCV001195217
RCV003891437
ClinVar Variation:
14307
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_002377.4:p.Asp294His
CA123861
NM_002386.4:c.880G>C