Canonical Allele Identifier: PA2826635376
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234483
ClinVar RCV Id: RCV000215890 RCV000225881 RCV000662360 RCV000569553 RCV004541361 RCV003998620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly318Ser
CA10577265
NM_001281494.2:c.952G>A