Canonical Allele Identifier: PA645381881
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 421501
ClinVar RCV Id: RCV000481556 RCV001190572 RCV000822224 RCV003470572 RCV004003355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro768Ala
CA068796
NM_000179.3:c.2302C>G