Canonical Allele Identifier: PA2826636395
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1793267
ClinVar RCV Id: RCV002426018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Phe556Leu
CA346754738
NM_001281494.2:c.1666T>C
CA346754753
NM_001281494.2:c.1668T>A
CA346754754
NM_001281494.2:c.1668T>G