Canonical Allele Identifier: PA193645
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 186021
ClinVar RCV Id: RCV000165541 RCV000410356 RCV000483409 RCV000685194 RCV002267913
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Tyr1038Cys
CA011594
NM_000179.3:c.3113A>G