Canonical Allele Identifier: PA132038
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43040

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1612Val
CA015389
NM_000257.4:c.4834C>G