Canonical Allele Identifier: PA098613
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 14097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu908Val
CA012953
NM_000257.4:c.2722C>G