Canonical Allele Identifier: PA915964605
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 647393
ClinVar RCV Id: RCV000801897 RCV003362950
ClinVar Variation Id: 1497615
ClinVar RCV Id: RCV002019478 RCV002407265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys646Asn
CA346750442
NM_000179.3:c.1938G>C
CA346750445
NM_000179.3:c.1938G>T