Canonical Allele Identifier: PA2825109903
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230895
ClinVar RCV Id: RCV004523009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu460Met
CA389050752
NM_000257.4:c.1378C>A