Canonical Allele Identifier: PA2826633421
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 583061
ClinVar RCV Id: RCV000707298 RCV001020752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu907Val
CA346760595
NM_001281493.2:c.2719C>G