Canonical Allele Identifier: PA645414679
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 429960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu216Val
CA389052341
NM_000257.4:c.646C>G