Canonical Allele Identifier: PA2580138655
Gene: MCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2360654
ClinVar RCV Id: RCV004205503

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001078846.2:p.Val720Met
CA3370009
NM_001085377.2:c.2158G>A