Canonical Allele Identifier: PA2825112087
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2822975
ClinVar RCV Id: RCV003749807
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys974Asn
CA389046573
NM_000257.4:c.2922G>T
CA389046574
NM_000257.4:c.2922G>C