Canonical Allele Identifier: PA2825112045
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2736077
ClinVar RCV Id: RCV003587420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu961Val
CA389046721
NM_000257.4:c.2881C>G