Canonical Allele Identifier: PA2825119173
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2497340
ClinVar RCV Id: RCV003213795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000255.2:p.Glu208Gly
CA374115077
NM_000264.5:c.623A>G