Canonical Allele Identifier: PA2825112699
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2644103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met1429Thr
CA041505
NM_000257.4:c.4286T>C