Canonical Allele Identifier: PA2573061716
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1317113
ClinVar RCV Id: RCV001758985
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu819Asp
CA346754082
NM_000179.3:c.2457G>C
CA346754083
NM_000179.3:c.2457G>T