Canonical Allele Identifier: PA2826627308
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1791086
ClinVar RCV Id: RCV002459837 RCV003759735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val679Leu
CA346754020
NM_001281492.2:c.2035G>C
CA346754021
NM_001281492.2:c.2035G>T