Canonical Allele Identifier: PA2829350929
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_002378.2:p.Gly525Arg
CA3370015
NM_002387.3:c.1573G>C
CA3370017
NM_002387.3:c.1573G>A