Canonical Allele Identifier: PA2825113142
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2093230
ClinVar RCV Id: RCV003018616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1632Ser
CA389037404
NM_000257.4:c.4894G>T