Canonical Allele Identifier: PA2825112143
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721955

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1022Met
CA389045731
NM_000257.4:c.3065A>T