Canonical Allele Identifier: PA2829395884
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1709049
ClinVar RCV Id: RCV002288333 RCV004005592
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002465.1:p.Thr671Ile
CA394868918
NM_002474.3:c.2012C>T