Canonical Allele Identifier: PA1139671730
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 924445
ClinVar RCV Id: RCV001185768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys213Asn
CA389052365
NM_000257.4:c.639G>T
CA389052366
NM_000257.4:c.639G>C