Canonical Allele Identifier: PA2825084954
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 823854
ClinVar RCV Id: RCV001020461 RCV001316018 RCV003467658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro12Ser
CA071083
NM_000179.3:c.34C>T