Canonical Allele Identifier: PA915970514
Gene: MCC HGNC NCBI

Linked Data

ClinVar Variation Id: 712996
ClinVar RCV Id: RCV000885064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001078846.2:p.Gly715Arg
CA3370015
NM_001085377.2:c.2143G>C
CA3370017
NM_001085377.2:c.2143G>A