Canonical Allele Identifier: PA132127
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val236Ala
CA016653
NM_000257.4:c.707T>C