Canonical Allele Identifier: PA658744488
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 491994
ClinVar RCV Id: RCV000583660 RCV000806695 RCV002466543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro293Ser
CA073534
NM_000179.3:c.877C>T