Canonical Allele Identifier: PA180955
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 177895

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys991Asn
CA013250
NM_000257.4:c.2973G>T
CA389046370
NM_000257.4:c.2973G>C