Canonical Allele Identifier: PA658680789
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455168
ClinVar RCV Id: RCV000551148 RCV004023716
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly661Asp
CA346750628
NM_000179.3:c.1982G>A