Canonical Allele Identifier: PA2826631212
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237151
ClinVar RCV Id: RCV000227011 RCV000483631 RCV000580465 RCV000662419 RCV003469132 RCV003998715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Met401Val
CA068470
NM_001281493.2:c.1201A>G