Canonical Allele Identifier: PA645380048
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 418322
ClinVar RCV Id: RCV000485848 RCV003593961
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asn455Lys
CA16617650
NM_000179.3:c.1365C>G
CA346744819
NM_000179.3:c.1365C>A