Canonical Allele Identifier: PA2826635349
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 186038
ClinVar RCV Id: RCV000165560 RCV000168072 RCV000479956 RCV002469035 RCV003462180 RCV003995427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Cys313Phe
CA009321
NM_001281494.2:c.938G>T