Canonical Allele Identifier: PA645378739
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233867
ClinVar RCV Id: RCV000213373 RCV000218922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu229Lys
CA10577257
NM_000179.3:c.685G>A