Canonical Allele Identifier: PA165541
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141475
ClinVar RCV Id: RCV000130018 RCV000410453 RCV000804545 RCV003997541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu226Gly
CA016211
NM_000179.3:c.677A>G