Canonical Allele Identifier: PA915970513
Gene: MCC HGNC NCBI

Linked Data

ClinVar Variation Id: 14203
ClinVar RCV Id: RCV000015267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001078846.2:p.Arg696Gln
CA250643
NM_001085377.2:c.2087G>A