Canonical Allele Identifier: PA2741920586
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2738232
ClinVar RCV Id: RCV003506626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Gly1176Trp
CA393085007
NM_005477.3:c.3526G>T