Canonical Allele Identifier: PA2826632832
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141299
ClinVar RCV Id: RCV000129766 RCV000409325 RCV000464994 RCV000515187 RCV000586138 RCV001175358 RCV003153418 RCV003467119 RCV003997523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro780Ser
CA012124
NM_001281493.2:c.2338C>T