Canonical Allele Identifier: PA2826630129
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1770709
ClinVar RCV Id: RCV002383366
ClinVar Variation Id: 1770711
ClinVar RCV Id: RCV002383368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Met150Ile
CA346744715
NM_001281493.2:c.450G>A
CA346744718
NM_001281493.2:c.450G>C
CA346744722
NM_001281493.2:c.450G>T