Canonical Allele Identifier: PA645495337
Gene: MYH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 260825

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060004.3:p.Leu1592Met
CA8390562
NM_017534.6:c.4774C>A