Canonical Allele Identifier: PA2499230375
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1046133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val236Phe
CA389052217
NM_000257.4:c.706G>T