Canonical Allele Identifier: PA2825113003
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230911
ClinVar RCV Id: RCV004523025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1557Asn
CA389037886
NM_000257.4:c.4671G>T
CA389037887
NM_000257.4:c.4671G>C